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: 85099•Ref: 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

Name

Acrostak AG

Address

Stegackerstrasse 14

Winterthur, Switzerland

Created Date

Jun 11, 2021

Authorized Representative

Name

QAdvis UK Ltd

Relationship Type

UK Responsible Person

Address

55-66 Frederick Street

Edinburgh, EH2 1LS, Scotland, United Kingdom

Postcode: EH2 1LS

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Other Products from Acrostak AG (2)

Peripheral angioplasty balloon catheter, basic

Type: General Medical Device

Registered: Nov 26, 2024

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Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

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

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