Tracheobronchial guidewire - UK MHRA Medical Device Registration

Tracheobronchial guidewire is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85010. The device is manufactured by bess pro gmbh from Germany, classified as General Medical Device. The authorized representative in the UK is Advena 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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Tracheobronchial guidewire

MHRA Device ID: 85010•Ref: 85010

Device Type

General Medical Device

Devices

Tracheobronchial guidewire

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Mar 22, 2024

Manufacturer Information

Name

bess pro gmbh

Address

Gustav-Krone-Straße 7

Berlin, Germany

Created Date

Apr 27, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Tracheobronchial guidewire - UK MHRA Medical Device Registration

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