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Coronary angioplasty balloon catheter, perfusing - UK MHRA Medical Device Registration

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.

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Coronary angioplasty balloon catheter, perfusing
MHRA Device ID: 85099โ€ขRef: 85099

Device Type

General Medical Device

Devices

Coronary angioplasty balloon catheter, perfusing

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 11, 2024

Manufacturer Information

Address

Stegackerstrasse 14

Winterthur, Switzerland

Created Date

Jun 11, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

55-66 Frederick Street

Edinburgh, EH2 1LS, Scotland, United Kingdom

Postcode: EH2 1LS

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