Coronary artery exposure retractor - UK MHRA Medical Device Registration
Coronary artery exposure retractor is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 98355. The device is manufactured by Terumo Cardiovascular Systems Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Terumo UK Ltd.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
General Medical Device
Devices
Coronary artery exposure retractor
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Oct 2, 2024
Address
125 Blue Ball Road
Elkton, Maryland, United States
Created Date
Apr 29, 2021
Name
Terumo UK LtdRelationship Type
Address
Otium House 2 Freemantle Road
Bagshot, Surrey, England, United Kingdom
Postcode: GU19 5LL
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Coronary artery exposure retractor
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Cardiotomy reservoir
Type: General Medical Device
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Coronary artery exposure retractor
Type: General Medical Device
Manufacturer: Terumo Cardiovascular Systems Corporation
Endoscopic electrosurgical electrode, bipolar, single-use
Type: General Medical Device
Manufacturer: Terumo Cardiovascular Systems Corporation
Extracorporeal membrane oxygenator
Type: General Medical Device
Manufacturer: Terumo Cardiovascular Systems Corporation
Surgical instrument assist arm system, manually-adjusted
Type: General Medical Device
Manufacturer: Terumo Cardiovascular Systems Corporation
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Type: General Medical Device
Manufacturer: Terumo Cardiovascular Systems Corporation
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Type: General Medical Device
Manufacturer: Terumo Medical Products (Hangzhou) Co., Ltd.

