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 70374. The device is manufactured by BIOTRONIK AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is BIOTRONIK UK 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: 70374•Ref: 70374

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Mar 5, 2024

Manufacturer Information

Name

BIOTRONIK AG

Address

Ackerstrasse 6

Bulach, Switzerland

Created Date

Mar 24, 2021

Authorized Representative

Name

BIOTRONIK UK LIMITED

Relationship Type

UK Responsible Person

Address

BIOTRONIK House, Avonbury Business Park

Bicester, United Kingdom

Postcode: OX26 2UA

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Other Products from BIOTRONIK AG (10)

Other Products from Same Authorized Representative (10)

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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