Fascial tissue dilator, single-use - UK MHRA Medical Device Registration

Fascial tissue dilator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 127261. The device is manufactured by UROMED Kurt Drews KG from Germany, 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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Fascial tissue dilator, single-use

MHRA Device ID: 127261•Ref: 127261

Device Type

General Medical Device

Devices

Fascial tissue dilator, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Sep 25, 2024

Manufacturer Information

Name

UROMED Kurt Drews KG

Address

Meessen 7/11

Oststeinbek, Germany

Created Date

Dec 22, 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

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Fascial tissue dilator, single-use - UK MHRA Medical Device Registration

Device Type

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