Needle guide, single-use - UK MHRA Medical Device Registration

Needle guide, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 192694. The device is manufactured by KOELIS from France, classified as General Medical Device. The authorized representative in the UK is Compliance Solutions (Lifesciences) 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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Needle guide, single-use

MHRA Device ID: 192694•Ref: 192694

Device Type

General Medical Device

Devices

Needle guide, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

May 14, 2024

Manufacturer Information

Name

KOELIS

Address

22 Chemin du Vieux Chêne

Meylan, France

Created Date

Jun 20, 2021

Authorized Representative

Name

Compliance Solutions (Lifesciences) Ltd

Relationship Type

UK Responsible Person

Address

Suite 10, Dunswood House 1 Dunswood Road Cumbernauld

Glasgow, United Kingdom

Postcode: G67 3EN

DJ Fang

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Other Products from KOELIS (4)

Other Products from Same Authorized Representative (10)

Needle guide, 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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