Stock Code
688016.SH
Stock Code
688016.SH
Company News
2023
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Groundbreaking Ceremony for Endovastec™ Global Headquarters and Innovation & Industrialization Base Project Successfully Held
17 Oct 2022
On October 17, 2022, the groundbreaking ceremony for the Global Headquarters and the Innovation & Industrialization Base Project of Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”, stock code: 688016.SH) was successfully held in Shanghai International Medical Zone (SIMZ), Zhangjiang Science City, Pudong District of Shanghai.
Endovastec™ Minos™ Abdominal Aortic Stent-Graft and Delivery System Receives Approval for Marketing in Colombia
02 Sept 2022
Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”) recently received registration approval from the Colombian National Institute for Drug and Food Surveillance (INVIMA) for the Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ System”). Colombia becomes the third Latin American country to approve the Minos™ System, after Brazil and Argentina. The Minos™ System obtained CE marking in 2019 and has been available in 12 overseas markets including Greece, Poland, the United Kingdom, Germany, Argentina, Brazil and other countries.
Endovastec™ Announces 2022 Interim Results
25 Aug 2022
Shanghai, China, 25 August 2022 — Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”) today announced the interim results of the Company and its subsidiaries for the six months ended 30 June 2022 (the “Reporting Period”).
Endovastec™ Reewarm™ PTX DCB PTA Catheter Receives Marketing Approval in Brazil
05 Jul 2022
Brasilia, Brazil, 4 July 2022 — Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”) today announced that it has received registration approval from the Brazilian Health Regulatory Agency (ANVISA) for its independently developed Reewarm™ paclitaxel (PTX) drug-coated balloon (DCB) percutaneous transluminal angioplasty (PTA) Catheter (“Reewarm™ PTX”).
Endovastec™ Receives MDSAP Certificate for Brazil and Japan
08 Apr 2022
Shanghai, China, 11 April 2022 — Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (Endovastec™) recently announced that it has received a Medical Device Single Audit Program (MDSAP) certificate from the Technischer Überwachungs-Verein (TÜV SÜD), an international notified body, certifying Endovastec™’s compliance with both ISO13485:2016 standards and the regulatory requirements in Brazil, and Japan, which lays the groundwork and provides the momentum for the company's global development.
Endovastec™ Announces Annual Results for 2021
31 Mar 2022
Shanghai, China, 29 March 2022 - Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (hereafter referred to as "Endovastec™" or the “Group”) today announced the annual results of the Company and its subsidiaries for the 12 months ended December 31, 2021 (hereafter referred to as the "Reporting Period"). In the reporting period, the Group recorded revenue of RMB 685 million, representing an increase of 45.59% as compared to the corresponding period of last year, with the net profit RMB 363 million, representing an increase of 45.15%. The net profit attributable to shareholders was RMB 316 million with an increase of 47.17%. The net profit excluding non-recurring gains and losses was RMB 289 million, an increase of 51.08%.
Hyperflex® Balloon Catheter by Endovastec™ Receives Marketing Approval in Japan
19 Mar 2022
Tokyo, Japan, 24 March 2022 — Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (Endovastec™) recently announced that it has received registration approval from Japan Pharmaceuticals and Medical Devices Agency (PMDA) for its independently-developed Hyperflex® Balloon Catheter (Hyperflex®) as the company’s first product approved for marketing in Japan. Hyperflex® obtained CE Mark in 2016 and is already available in overseas markets in South America and Asia.
First Clinical Implantation of Endovastec™’s Hercules®-LP Thoracic Stent Graft System Completed in India
03 Mar 2022
Kochi, India - Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (Endovastec™) has completed the first clinical implantation of its independently developed Hercules® Low Profile Thoracic Stent Graft and Delivery System (Hercules®-LP Stent Graft System) in India. This is the first product from Endovastec™ which has been approved for marketing and used in a clinical setting in India, the thirteenth market for the Hercules®-LP Stent System, following China, Brazil, Italy, the United Kingdom, and Turkey.
Endovastec™ Talos™ Thoracic Stent Graft System Receives NMPA Approval for Marketing
12 Jan 2022
Shanghai, China—Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (Endovastec™) recently received a registration certificate from China’s National Medical Products Administration (NMPA) for its independently developed Talos™ Thoracic Stent Graft System (Talos™).
Endovastec™ Debuts at Pan-American Congress on Vascular and Endovascular Surgery
15 Oct 2021
Rio de Janeiro, Brazil—Recently, Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”), debuted at the XVI Pan American Congress on Vascular and Endovascular Surgery (PAN 2021) with two flagship products, the Castor™Branched Aortic Stent-Graft System (“Castor™ Stent”) and the Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”). As the most prestigious and authoritative congress for endovascular surgery in Latin America, the online congress was attended by about 40 experts to discuss various hot topics related to aortic aneurysm, aortic arch, aortoiliac occlusive disease, subinguinal and distal venous thrombosis, COVID-19 complications, varicose vein surgery, and carotid artery surgery, among others.
Clinical Trial Enrollment Completed for the First Endovastec™ Venous Stent
10 Oct 2021
Beijing, China—The final procedure of the pre-market multicenter clinical trial for the Vflower® Venous Stent System, a braided venous stent independently developed by Shanghai MicroPort Endovascular MedTech （Group）Co., Ltd. (“Endovastec™”), a subsidiary of MicroPort Scientific Corporation (00853.HK), was recently completed, marking the completion of enrollment in this program. The clinical trial for the Vflower® Venous Stent System is a prospective, multi-center, single-arm nationwide clinical study led by Peking Union Medical College Hospital in conjunction with The Affiliated Hospital of Qingdao University and 12 medical centers as co-participators in China. It took only 10 months from the first implantation to the enrollment completion.
Products Complete First Implantations in the UK Following Endovastec’s Entry into the UK Market
03 Sept 2021
Hull and Doncaster, United Kingdom—Shanghai MicroPort Endovascular MedTech(Group) Co., Ltd. (“Endovastec™”), announced recently that the first implantations of the Castor™ Branched Aortic Stent-Graft System (“Castor™ Stent”), Hercules™ Low Profile Thoracic Stent Graft and Delivery System (“Hercules™-LP Stent Graft System”) and the Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”) have been successfully completed in the United Kingdom. The UK is the sixth overseas market where the Castor™ Stent is available, after Poland, Spain, Argentina, Italy and Brazil, is the ninth overseas market for the Hercules™-LP Stent Graft System, after Argentina, Brazil, Poland, Georgia, Italy, Spain, Germany and Turkey, and is the twelfth overseas market for the Minos™ Stent Graft System, after Greece, Poland, Spain, Germany, Italy, Switzerland, Argentina, Croatia, Hungary, Brazil and the Czech Republic.
Endovastec™ Minos™ Stent Graft System Completes First Clinical Implantation in Czech Republic
02 Aug 2021
Prague, Czech Republic—The first implantation of the Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”), a product self-developed by Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”), was completed in the Czech Republic. This marks the eleventh overseas market that the Minos™ Stent Graft System has entered, after Greece, Poland, Spain, Germany, Italy, Switzerland, Argentina, Croatia, Hungary and Brazil.
Endovastec™ Received ISO 50001 Energy Management System Certificate
02 Aug 2021
Shanghai, China - Shanghai MicroPort Endovascular MedTech （Group）Co., Ltd. (Endovastec™), has obtained the ISO 50001:2018 Energy Management System Certificate after passing the assessment by the Conformity Assessment Certification Body. To date, Endovastec™ has developed an increasingly comprehensive management system after having passed a series of system certifications including for quality management, environmental management, occupational health and safety management, brand cultivation management, and intellectual property management, as well as the CNAS (China National Accreditation Service for Conformity Assessment) laboratory certification.
Endovastec™ Successfully Held First International TEVAR MasterClass
13 Jun 2021
Beijing, China—Recently, Shanghai MicroPort Endovascular MedTech(Group) Co., Ltd. (“Endovastec™”), successfully held the first International Thoracic Endovascular Aortic Repair (TEVAR) MasterClass. This online class invited ten experts from China and Europe, including Professor Chang Shu, Director of the Vascular Surgery Center of Fuwai Hospital, Chinese Academy of Medical Sciences, National Center for Cardiovascular Diseases and Prof. Franco Grego, the incumbent President of the European Society of Cardiovascular Surgery (ESCVS) and Director of Vascular Surgery Department at Padua University Hospital. During the Masterclass, the experts conducted in-depth exchanges and discussions on the cutting-edge developments and academic insights on TEVAR. More than a hundred participants watched the live streaming and participated in discussions online.
First Implantation of Endovastec™ Minos™ Completed in Brazil
05 Jun 2021
São Paulo, Brazil—Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”), a product developed by Shanghai MicroPort Endovascular MedTech(Group) Co., Ltd. (“Endovastec™”), was used in Brazil for the first time in a recently completed case. This marks the tenth overseas market that the Minos™ Stent Graft System has entered, after Greece, Poland, Spain, Germany, Italy, Switzerland, Argentina, Croatia and Hungary.
First Implantation of Endovastec™ Castor™ Completed in Argentina
05 Mar 2021
Tandil, Argentina—The first implantation of the Castor® Branched Aortic Stent-Graft System (the “Castor™ Stent”) developed by Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”), a subsidiary of Shanghai MicroPort Medical (Group) Co., Ltd. (00853.HK), was completed in Argentina, marking the product’s presence in the third overseas market after Poland and Spain, and the first one in South America.
Reewarm™ PTX Drug Coated PTA Balloon Catheter Received EU CE Marking Certification
14 Dec 2020
Shanghai, China—Reewarm™ PTX Drug Coated PTA Balloon Catheter (“Reewarm™ PTX DCB Catheter”) developed by Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”) has recently obtained the CE Marking certification issued by the European Union. Previously, the product has received the registration certificate issued by China’s National Medical Products Administration (NMPA) in April 2020.
Endovastec™ Minos™ Completed First Clinical Implantation in Hungary
14 Dec 2020
Debrecen, Hungary—The Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”), which is developed by Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”) and now available in nine overseas markets, successfully completed its first implantation in Hungary in a recent operation.
Endovastec™ Accredited as“Shanghai Enterprise Technology Center”
27 Nov 2020
Shanghai, China—Shanghai MicroPort Endovascular MedTech（Group）Co., Ltd. (Endovastec™) was accredited as a “Shanghai Enterprise Technology Center” for its outstanding performance in developing technical talents and efforts in technological innovation, in the 2020 list of Municipal Enterprise Technology Centers in Shanghai (batch 26) recently released by Shanghai Municipal Economy and Information Technology Commission (SHEITC).
Endovastec™ Castor™ Entered First Overseas Market
23 Nov 2020
Szczecin, Poland, December 11, 2020 — The first implantation of the Castor™ Branched Aortic Stent-Graft and Delivery System (“Castor™”), developed by Shanghai MicroPort Endovascular MedTech（Group）Co., Ltd. (“Endovastec™”), was successfully completed in Poland in 29 October. Castor™ is the world’s first stent-graft system for simultaneous aorta and aortic arch repair through minimally invasive treatment.
speX Support Catheter Obtained NMPA Registration Certificate
10 Nov 2020
Shanghai, China—The speX Support Catheter distributed by Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (Endovastec™) recently received a registration certificate from the National Medical Products Administration (NMPA).
Endovastec™ Completed the First Implantation for Minos™ in Argentina
09 Nov 2020
Buenos Aires, Argentina – Shanghai MicroPort Endovascular MedTech (Group) Co., Ltd. (“Endovastec™”) recently successfully completed the first case for its Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”) in Argentina. It is the seventh international market outside of China where Minos™ Stent Graft System has entered after Greece, Poland, Spain, Germany, Italy and Switzerland, also the first country in South America.
Endovastec™ Completed the First Implantation of Minos™ in Spain
17 Jul 2020
Barcelona, Spain——July 15th, 2020. The Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”), which is produced by Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”), was successfully implanted in a patients with abdominal aortic aneurysm (AAA) in Spain. Spain is the third overseas market of Minos™ Stent Graft System after Greece and Poland.
Endovastec™ Completed the First Implantation of Minos™ in Poland
12 Jun 2020
Opole, Poland — June 8th, 2020. The Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”), which is produced by Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”), was successfully implanted in three patients with abdominal aortic aneurysm (AAA) in Poland. Poland is the second overseas market of Minos™ Stent Graft System after Greece.
Endovastec™ Won 2019 Shanghai Municipal Quality Management Prize
02 Mar 2020
Shanghai, China – Shanghai MicroPort Endovascular MedTech Co., Ltd. ("Endovastec™") was recently awarded the 2019 Shanghai Municipal Quality Management Prize ("Prize"). The winners of the Prize were announced after the procedure including formal review, dossier assessment, panel review, on-site verification, result approval and online pre-release.
Endovastec™ Won "Pudong New Area Quality Gold Prize”
10 Jan 2020
Shanghai, China – Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”) was recently awarded the “Pudong New Area Quality Gold Prize” (“the Prize”) after a panel announced the results of the panel review and public inputs done for the 3rd Pudong New Area Government Quality Prizes.
Endovastec™ Completed the First Implantation of Minos™ Outside of China
04 Mar 2020
Thessaloniki, Greece – The Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™”), which is produced by Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”), was successfully implanted in a patient with abdominal aortic aneurysm (AAA) in Greece recently. Professor Georgios A. Pitoulias from General Hospital of Thessaloniki “G. Gennimatas - Agios Dimitrios” was the first expert in Europe to try this product. The case marked the first implantation of Minos™ Stent Graft System outside of China since the device received CE Mark in September 2019.
Minos™ was Selected as Shanghai innovative Biomedical Products in 2018-2019
12 Oct 2019
Shanghai, China——On September 30, 2019, Shanghai Science and Technology Commission published a publicity list of the results of the evaluation of Shanghai innovative biomedical products in 2018-2019. And Minos™ Abdominal Aortic Stent-Graft and Delivery System (“Minos™ Stent Graft System”) independently developed by Shanghai MicroPort Endovascular MedTech Co., Ltd (“Endovasctec™”) was successfully selected. Minos™ Stent Graft System was Approved special medical device approval process in 2017, gained NMPA approval in March and CE certificate in September 2019. And its post-marketing clinical study was selected for the 2019 “Science and Technology Innovation Action Plan” project in the field of cooperation between industry, education, research and medicine in Shanghai.
Endovasctec™ Won the 2019 Shanghai Key Product Quality Research Achievement Award
12 Oct 2019
Shanghai, China——On September 30, 2019, Shanghai Administration Bureau of Market Supervision and Shanghai Municipal Economic and Information Commission co-organized an exchanging meeting of the 2019 Shanghai key product quality research work experience, which announced the results of the 2019 Shanghai key product quality research projects and individuals. Industrialization upgrading project of Hercules™ Low Profile Thoracic Stent-Graft System was awarded the third prize of the 2019 Shanghai key product quality research achievement award for its technological innovation and industrial management advantages.
The Post-marketing Clinical Study of Minos™ was Selected for 2019 “Science and Technology Innovation Action Plan” Project in the Field of Cooperation
30 Sept 2019
Shanghai, China——As a clinical demonstration application research topic for innovative medical devices, the post-marketing clinical study of Minos™ Abdominal Aortic Stent-Graft and Delivery System, which was co-declared by Shanghai MicroPort Endovascular MedTech Co., Ltd (“Endovasctec™”), Zhongshan Hospital of Fudan University and Renji Hospital of Shanghai Jiaotong University, was selected for the 2019 “Science and Technology Innovation Action Plan” project in the field of cooperation between industry, education, research and medicine in Shanghai.
Minos™ Gained CE Certificate
17 Sept 2019
Shanghai, China——Minos™ Abdominal Aortic Stent-Graft and Delivery System ( “Minos™”) independently developed by Shanghai MicroPort Endovascular MedTech Co., Ltd (“Endovasctec™”) successfully gained CE certificate on September 12, 2019. It is the third CE certificate product following the Hercules™ Balloon Inflation Catheter and Reewarm™ PTA Balloon Dilatation Catheter, and the first CE certificate for the aortic stent graft products.
Endovastec™ was Listed on the STAR Market of the Shanghai Stock Exchange
22 Jul 2019
Shanghai, China - Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”, or “the Company”) was listed on the STAR Market (Stock code: 688016) of the Shanghai Stock Exchange on July 22, 2019, becoming one of few medical device companies in the first batch of 25 companies to be listed on the market.
Endovastec™ Gained NMPA Approval for Minos™Abdominal Aortic Stent-Graft and Delivery System
25 Mar 2021
Shanghai MicroPort Endovascular MedTech Co., Ltd.（Endovastec™）recently announced that it has gained China NMPA (National Medical Products Administration) approval for its in-house developed Minos™Abdominal Aortic Stent-Graft and Delivery System (Minos™), which marked a formal clearance for entering the Chinese market.
"Hercules®" Trademark Granted Entry into the List of the Third Batch of Major Protected Trademarks of Shanghai Municipality
05 Feb 2019
Shanghai, China - The Shanghai Municipal Administration of Market Regulation recently published the List of the Third Batch of Major Protected Trademarks of Shanghai Municipality (“the List”). The “Hercules®” trademark of Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”) was granted the entry into the List and rated as one of the third batch of Major Protected Trademarks of Shanghai Municipality.
A Patent of Hercules™-LP Won Shanghai Intellectual Property Innovation Award
08 Nov 2019
Shanghai, China – Recently, results of Shanghai Intellectual Property Innovation Award were released. This activity was carried out jointly by Shanghai Municipal Bureau of human resources and social security, Shanghai Intellectual Property Administration. A patent named Stent-Graft System and its usage of Hercules™ Low-Profile Thoracic Stent-Graft System（“Hercules™-LP”）,which belongs to Shanghai MicroPort Endovascular MedTech Co., Ltd (“Endovasctec™”), won second prize of patent and trademark in the Shanghai Intellectual Property Innovation Award with its cultivation, transformation and industrialization of high-value intellectual property. Endovasctec™ was awarded the Shanghai Patent Work Pilot Enterprise in 2017.
Minos™ Entered 2019 Shanghai Municipality Recommendation Directory for Innovative Products
04 Dec 2019
Shanghai, China – Shanghai Municipal Commission of Economy and Informatization published the 2019 Shanghai Municipality Recommendation Directory for Innovative Products recently. The Minos™ Ultra-Low Profile Abdominal Aortic Aneurysm Stent Graft System (“Minos™ Stent Graft”), which is self-developed by Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”), was successfully granted entry into the directory.
Castor™ Granted Entry into the 2018 Shanghai Municipality Innovative Product Recommendation List
11 Jan 2019
Shanghai, China – Recently, Shanghai Municipal Commission of Economy and Informatization published the 2018 Shanghai Municipality Innovative Product Recommendation List (“the Recommendation List”). The Castor™ Branched Aortic Stent-Graft System ("Castor™"), which was independently developed by Shanghai MicroPort Endovascular MedTech Co., Ltd. (Endovastec™), was granted entries into the list.
Castor™ Included in "2018 Shanghai Innovative Product Recommendation List"
01 Dec 2018
Shanghai, China——Recently, Shanghai Municipal Commission of Economy and Informatization released the “2018 Shanghai Innovative Product Recommendation List”(Recommendation List). The product in-house developed by Shanghai MicroPort Endovascular MedTech Co., Ltd. (“Endovastec™”), Castor Branched Aortic Stent-Graft System (“Castor”) was successfully selected. Castor launched in June of 2017 after it Entered “Green Path”in 2015.
Endovastec™ Selected as "2018 Shanghai Science and Technology Little Giant Enterprise"
01 Nov 2018
Recently， Shanghai MicroPort Endovascular MedTech Co., Ltd.( Endovastec™) was listed as “2018 Shanghai Science and Technology Little Giant Enterprise”. In future, the selected companies will gain funding from city or district (county) governments based on the companies' independent innovation plans.Before then, MicroPort® Endovascular was successfully Selected as “2016 Shanghai Science and Technology Little Giant Enterprise(for Cultivation)”, and passed the project acceptance inspection in 2018.
FONTUS™ Single-branched Stent Graft System in Surgical Operation Enters “Green Path”
15 Aug 2018
Shanghai, China - Recently, FONTUS™ Single-branched Stent Graft System in Surgical Operation (“FONTUS™”), which is independently developed by Shanghai MicroPort Endovascular MedTech Co., Ltd. (“MicroPort Endovascular”), has passed the review of China State Drug Administration (SDA) and entered the special review and approval procedure for innovative medical devices, which is also known as the Green Path.
MicroPort® Endovascular Awarded 2017 Shanghai Brand Cultivation Demonstration Enterprise
12 Sept 2018
Shanghai, China – On April 9, MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") was awarded "2017 Shanghai Brand Cultivation Demonstration Enterprise" by Shanghai Municipal Commission of Economy and Information.
MicroPort® Endovascular Hercules™ Series Products Gained Regulatory Approval in Colombia
08 Feb 2018
Bogota, Colombia - MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") obtained the regulatory approval from Colombia's health authority INVIMA for its in-house developed Hercules™-T Low Profile Stent-Graft ("HT-LP"), Hercules™ Bifurcated Stent-Graft System and Delivery System, and Hercules™ Balloon Dilation Catheter. This is the first time for MicroPort® Endovascular's products to gain regulatory approval in Colombia. Previously, the three products have received approval in Brazil, Argentina, Peru, Thailand, Indonesia, and the Philippines.
MicroPort®Endovascular Gained its First State Science and Technology Progress Award
25 Jan 2018
Shanghai, China – On January 8, the project of "Key Technology Development and Large-scale Industrialization of Aortic Stent Graft Products", jointly developed by Shanghai MicroPort (Medical) Group Co., Ltd. ("MicroPort®"), its subsidiary MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), and Beijing Anzhen Hospital of Capital Medical University, won the second prize of State Science and Technology Progress Award. It is the first State Science and Technology Progress Award earned by MicroPort® Endovascular.
Altura™ Endograft System Granted CFDA Green-Path
09 Jan 2018
Shanghai, China – On December 6, Altura™ Endograft System ("Altura™"), distributed by MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort®Endovascular") and developed by UK-based Lombard Medical, Inc. ("Lombard Medical"), was granted to enter the special Green-Path by China Food and Drug Administration ("CFDA"), which is rapid-track of review and approval procedure for innovative medical devices.
MicroPort® Endovascular's HT-LP Included in 2017 Shanghai Innovative Product Recommendation List
14 Nov 2017
Shanghai, China – Hercules™-T Low Profile Stent-Graft ("HT-LP"), in-house developed by MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), was recently included in the 2017 Shanghai Innovative Product Recommendation List ("Recommendation List") according to an announcement recently released by Shanghai Municipal Commission of Economy and Informatization. Such honor is expected to benefit the commercialization and industrialization of HT-LP.
MicroPort® Endovascular Hosted Product Launch of Castor™
15 Oct 2017
Shanghai, China – From October 12 to October 14, MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") attended the Endovascology 2017 and hosted product launch of Castor™ Branched Aortic Stent-Graft System ("Castor™"). The conference aims to bring in the latest advancement and cutting-edge technology to China and to showcase the achievements in China's endovascular industry. More than 2,500 industry experts from over 40 countries including China, US, Canada, South Korea, Australia, and Egypt attended the congress to discuss about hot issues in the vascular surgery field worldwide.
First Post-market Implantation of Castor™ Successfully Completed
10 Oct 2017
Suzhou, China – The first post-market implantation of Castor™ Branched Aortic Stent-Graft System ("Castor™"), in-house developed by MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), was recently successfully completed by Director Xiaoqiang Li of the Second Affiliated Hospital of Soochow University. The product gained the regulatory approval from China Food and Drug Administration in June 2017 to officially enter the China market.
Talos™ Gained CFDA Green-Path
28 Sept 2017
Shanghai, China – On September 27, Talos™ Thoracic Stent Graft System ("Talos™"), self-developed by MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), was approved to enter the special Green-Path by China Food and Drug Administration ("CFDA"), which is rapid-track of review and approval procedure for innovative medical devices. The Green-Path will significantly expedite the approval time and meanwhile it demonstrated the recognition of Chinese government authorities in Talos™.
MicroPort® Endovascular Listed as 2017 Shanghai Patent Affairs Pilot Enterprise
12 Sept 2017
Shanghai, China - MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") was recently listed as "2017 Shanghai Patent Affairs Pilot Enterprise" by Shanghai Intellectual Property Administration and will receive fund from Shanghai government and Pudong district government. Shanghai Intellectual Property Administration started to accept applications of patent demonstration/pilot enterprises since February and selected 95 companies as "2017 Shanghai Patent Affairs Pilot Enterprises" after expert review, group discussion, and authority approval.
Reewarm™ Gained CFDA Approval
24 Jul 2017
Shanghai, China - MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") recently obtained the regulatory approval from China Food and Drug Administration ("CFDA") for its in-house developed Reewarm™ PTA Balloon Catheter ("Reewarm™"). Reewarm® is designed to treat atherosclerosis-caused stenosis and occlusive disease in artery below groin, such as iliac artery, femoral artery, superficial femoral artery, popliteal artery, inferior genicular artery. It provides pre-expansion of the narrowed vascular lumen for future treatment.
Castor™ Gained CFDA Approval
11 Jul 2017
Shanghai, China - Castor™ Branched Aortic Stent-Graft System ("Castor™"), in-house developed by Shanghai MicroPort Medical (Group) Co., Ltd ("MicroPort®"), recently obtained the regulatory approval from China Food and Drug Administration ("CFDA"). It is the fourth device of MicroPort® that gained the CFDA approval through the CFDA Green Path for innovative medical devices.
MicroPort® Endovascular was Listed as 2016 Shanghai Pudong New Area Enterprise Institution
21 Apr 2017
Shanghai, China – Shanghai Pudong New Area Technology and Finance Committee recently released the list of Enterprise R&D Institutions in Pudong New Area, and MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") was listed among the 38 R&D institutions.
Development and Industrialization of Key Technologies in Minimally Invasive Treatment of Aortic Diseases Wins First Prize of Shanghai Science and Technology Progress Award
23 Oct 2017
Shanghai, China – On March 22, the Project of "Development and Industrialization of Key Technologies in Minimally Invasive Treatment of Aortic Diseases," jointly developed by Shanghai MicroPort (Medical) Group Co., Ltd ("MicroPort®"), its subsidiary MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), Beijing Anzhen Hospital of Capital Medical University, and Changhai Hospital of the Second Military Medical University, won the First Prize of Shanghai Science and Technology Progress Award.
MicroPort® Endovascular Awarded the Title of 2016 Shanghai Specialized, Sophisticated, Distinctive, Innovative SMEs
11 Jan 2017
Shanghai, China – On January 9, MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), the subsidiary of Shanghai MicroPort Medical (Group) Co., Ltd. ("MicroPort®"), was awarded the title of "2016 Shanghai Specialized, Sophisticated, Distinctive, Innovative Small- and Medium-sized Enterprises ("SMEs")" by Shanghai Municipal Commission of Economy and Informatization.
Hercules™ was Awarded 2016 Shanghai Top-Brand Product
03 Jan 2017
Shanghai, China – On December 31, Hercules™ Stent Graft and Delivery System, in-house developed by MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), was awarded 2016 Shanghai Top-Brand Product, according to a list released by Shanghai Top Brand Recommendation Committee of Shanghai Municipal Bureau of Quality and Technical Supervision. The award is to honor well-known products and brands with industry-leading position, high customer satisfaction and great development potential.
MicroPort® Endovascular Received CE Mark Approval for Hercules™ Inflation Catheter and Reewarm™ PTA Balloon Catheter
15 Dec 2016
Shanghai, China – On December 13, MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") in-house developed Hercules™ Balloon Inflation Catheter and Reewarm™ PTA Balloon Catheter were both granted CE mark approval. It is the first CE mark approvals MicroPort® Endovascular has received, to successfully have its products registered in European Union countries, marking the first solid step to enter the European Union markets.
MicroPort® Endovascular was Selected as 2016 Shanghai Science and Technology Little Giant Enterprise (for Cultivation)
18 Nov 2016
Shanghai, China – On November 17, Shanghai MicroPort Medical (Group) Co., Ltd. ("MicroPort®") announced that its subsidiary MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") was listed as "2016 Shanghai Science and Technology Little Giant Enterprise (for Cultivation)" by Science and Technology Commission of Shanghai Municipality and Shanghai Municipal Commission of Economy and Informatization. The selected company will gain funding from city or district (county) governments based on the companies' independent innovation plans. Founded in 2010 and 2013 in Shanghai, MicroPort® Endovascular primarily focus on the development, manufacture, and marketing of the interventional medical devices respectively for the treatment of electrophysiological diseases, and peripheral-vascular- and endovascular-related diseases. Its device is widely used in China's top hospitals and has been exported to many overseas countries and regions. MicroPort® Endovascular was selected as 2015 Shanghai High- and New-Technology Enterprise.
MicroPort® Endovascular Received Outstanding Contribution to Performance Improvement Award of ISPI-China
02 Nov 2016
Beijing, China - On October 27, MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular") was granted the "Outstanding Contribution to Performance Improvement Award" and its project "PLUS"（Portfolio Life-cycle United Stimulation）was granted the "Best Practice of Performance Improvement Award" by the International Society for Performance Improvement – China ("ISPI-China") in the 6th China Performance Improvement Forum held in Beijing. The forum aims to distribute the latest updates related with performance improvement and provides a platform for companies that stand out for performance improvement to share their experience and development stories.
Minos™ Completed Patient Enrollment of Pre-market Clinical Trials
18 Sept 2016
Shanghai, China - Minos™ Ultra Low Profile Abdominal Aortic Aneurysm ("AAA") Stent-Graft and Delivery System ("Minos™ Ultra Low Profile AAA Stent-Graft"), in-house developed by MicroPort Endovascular (Shanghai) Co., Ltd. ("MicroPort® Endovascular"), completed patient enrollment of pre-market clinical trials in assessing the safety and efficacy of Minos™ Ultra Low Profile AAA Stent-Graft in the treatment of AAA.
MicroPort® Awarded Shanghai Pudong New Area Top 20 Outstanding Contributor to Advanced Manufacturing Industry
29 Mar 2016
Shanghai, China – On March 29, Shanghai MicroPort Medical (Group) Co., Ltd. ("MicroPort®") was awarded the Top 20 Outstanding Contributors to Advanced Manufacturing Industry of Shanghai Pudong New Area during the "2016 Awarding Ceremony of Outstanding Contributor to Economic Growth of Pudong New Area," fully demonstrating government authority's recognition of the achievements MicroPort® made in 2016.
Reewarm™ PTX Granted Green Channel Status for CFDA Approval
19 Feb 2016
MicroPort® Endovascular Recognized as One of Shanghai's the First Group of High-tech Enterprise
20 Oct 2015
Shanghai, China -- recently, the Shanghai Municipal Office of Accreditation For Shanghai's High-tech Enterprises published a list of Shanghai's first batch of high-tech enterprises for year 2015. Shanghai MicroPort Endovascular (Shanghai) Co ("MicroPort® Endovascular")was selected in the list, won the "high-tech enterprise" certificate, and will enjoy the benefit of the preferential policy that will deduct the income tax, equal to about 15% corporate income during the next three years. This recognition was jointly determined by the Shanghai Municipal Science and Technology Commission, Shanghai Municipal Finance Bureau, Shanghai Municipal State Tax Bureau and the Shanghai Municipal Bureau of Local Taxation, and announced to the public by the Shanghai Municipal High-tech Enterprises Identified Office.
Hercules™ Balloon Inflation Catheter Gained Market Launch Approval in Brazil
20 Aug 2015
MicroPort Endovascular (Shanghai) Co ("MicroPort® Endovascular") recently gained the registration certificate for its in-house developed Hercules™ Balloon Inflation Catheter from Brazil's National Health Surveillance Agency.
MicroPort® Hosted 2015 Annual Distributor Conference
15 May 2015
Shanghai, China – 15 May, 2015 – Shanghai MicroPort Medical (Group) Co ("MicroPort") hosted 2015 Annual Distributor Conference on May 14 in its Shanghai headquarters to promote its products to nationwide distributors. About 400 distributors attended the meeting.
MicroPort® Endovascular Completed First Application of Reewarm™ PTX Drug Coated PTA Balloon Catheter
24 Mar 2015
Shanghai, China – 24 March, 2015 – MicroPort Endovascular (Shanghai) Co ("MicroPort Endovascular") recently successfully completed its first clinical application of Reewarm™ PTX Drug Coated PTA Balloon Catheter ("Reewarm™ PTX") in the middle segment of superficial artery. The Reewarm™ PTX clinical trial is a prospective, multi-center, single blind, randomized, controlled study, comparing drug coated balloon ("DCB") versus standard balloon angioplasty for the treatment of femoropopliteal arteries, which is expected to enroll 200 patients (1:1) in 11 centers in China.
MicroPort® Endovascular Released Six-month Follow-up Data of Castor™
09 Feb 2015
Shanghai, China – 9 February, 2015 – MicroPort Endovascular (Shanghai) Co ("MicroPort Endovascular") recently released the six-month follow-up data of its in-house developed Castor™ Branched Aortic Stent Graft System ("Castor™") on Vascular News, an important source for news, views, comment and controversy in the vascular industry.
MicroPort® Endovascular Completed Enrollment of Pre-market Clinical Trial for Reewarm18
20 Dec 2014
MicroPort Endovascular (Shanghai) Co ("MicroPort® Endovascular") recently completed the enrollment of pre-market clinical trial for its first-generation Reewarm18 Peripheral Balloon Dilation Catheter ("Reewarm18") to prove its safety and efficacy.
Castor™ was Selected as Key Project of National Program
30 Nov 2014
Castor™ Thoracic Branch Stent-Graft System ("Castor™"), an endovascular device developed by MicroPort Endovascular (Shanghai) Co, a subsidiary of Shanghai MicroPort Medical (Group) Co ("MicroPort"), was successfully selected as one project of the National Key Technology R&D Program for China's 12th Five-Year Plan in November.
First Clinical Implantation of Ultra Low Profile Completed
13 Nov 2014
Ultra Low Profile AAA Stent-Graft System ("Ultra Low Profile"), an endovascular device in-house developed by MicroPort Endovascular (Shanghai) Co ("MicroPort Endovascular"), a subsidiary of Shanghai MicroPort Medical (Group) Co ("MicroPort"), recently completed its first clinical implantation in Shanghai-based Zhongshan Hospital.
CRONUS™ Stent Graft System In Surgical Operation won the second prize of Pudong Scientific and Technological Achievements.
05 Oct 2014
Shanghai, China – 30 October, 2014 - CRONUS™ Surgical Stent Graft System ("CRONUS™"), an endovascular device of Shanghai MicroPort Medical (Group) Co., Ltd. ("MicroPort"), was recently granted the second prize of scientific and technological achievements by Pudong New Area Science and Technology Commission of Shanghai Municipality.
Hercules™ Balloon Inflation Catheter Received CFDA Certificate
17 Oct 2013
Recently, Hercules™ Balloon Inflation Catheter, independently developed by MicroPort and its subsidiary MicroPort Endovascular (Shanghai) Co., Ltd., received certificate from China Food and Drug Administration (CFDA). Hercules™ Balloon Dilatation Catheter literary filled the gap in the domestic-made large balloon market and broke the dependence on the foreign-made products. The device effectively addresses the endoleak during the endovascular treatment for the aortic aneurysm or dissection.
Hercules™-B Bifurcated Stent-graft and Delivery System Honored with 2013 National Key New Project
28 Sept 2013
Recently, MicroPort's Hercules™-B Bifurcated Stent-graft and its delivery system were honored with 2013 National Key New Project. It is the 5th consecutive years in which MicroPort has receive the certificate.
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