Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

Cardiac/peripheral vascular guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 175683. The device is manufactured by Angiomed GmbH&Co. Medizintechnik KG from Germany, classified as General Medical Device. The authorized representative in the UK is Becton, Dickinson U.K. Limited.

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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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 175683•Ref: 175683

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Dec 22, 2023

Manufacturer Information

Name

Angiomed GmbH&Co. Medizintechnik KG

Address

Wachhausstrasse 6

Karlsruhe, Germany

Created Date

Feb 15, 2021

Authorized Representative

Name

Becton, Dickinson U.K. Limited

Relationship Type

UK Responsible Person

Address

1030 Eskdale Road Winnersh Triangle, Wokingham

Winnersh, England, United Kingdom

Postcode: RG41 5TS

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Other Products from Angiomed GmbH&Co. Medizintechnik KG (10)

Other Products from Same Authorized Representative (10)

Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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