Gastro-urological guidewire, single-use - UK MHRA Medical Device Registration

Gastro-urological guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 183160. The device is manufactured by Rocamed France from France, classified as General Medical Device. The authorized representative in the UK is International Associates 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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Gastro-urological guidewire, single-use

MHRA Device ID: 183160•Ref: 183160

Device Type

General Medical Device

Devices

Gastro-urological guidewire, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Sep 17, 2024

Manufacturer Information

Name

Rocamed France

Address

Parc d’activités de Signes Allée de Stockholm

Signes, France

Created Date

Dec 13, 2023

Authorized Representative

Name

International Associates Limited

Relationship Type

UK Responsible Person

Address

38 Queen Street

Glasgow, Scotland, United Kingdom

Postcode: G1 3DX

DJ Fang

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Other Products from Rocamed France (7)

Other Products from Same Authorized Representative (10)

Gastro-urological 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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