Coronary angioplasty balloon catheter, perfusing
United Kingdom·General Medical Device·Acrostak AG·Registered Nov 26, 2024- Device ID
- 85099
- MHRA Reference Number
- 85099
- Date Registered
- Nov 26, 2024
- Last Updated
- Jul 11, 2024
- Device Type
- General Medical Device
- Devices
- Coronary angioplasty balloon catheter, perfusing
- Type
- Class III
- Name
- Acrostak AG
- Address
- Stegackerstrasse 14 Winterthur, Switzerland
- Created Date
- Jun 11, 2021
- Name
- QAdvis UK Ltd
- Relationship Type
- UK Responsible Person
- Address
- 55-66 Frederick Street Edinburgh, EH2 1LS, Scotland, United KingdomPostcode: EH2 1LS
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by QAdvis UK Ltd in the UK
Coronary angioplasty balloon catheter, perfusing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85099. The device is manufactured by Acrostak AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is QAdvis 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.