Dermal tissue reconstructive material, synthetic mineral - UK MHRA Medical Device Registration

Dermal tissue reconstructive material, synthetic mineral is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 78888. The device is manufactured by Cytophil, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is QCS International 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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Dermal tissue reconstructive material, synthetic mineral

MHRA Device ID: 78888•Ref: 78888

Device Type

General Medical Device

Devices

Dermal tissue reconstructive material, synthetic mineral

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Cytophil, Inc.

Address

2485 Corporate Circle Suite 2

East Troy, WI, United States

Created Date

Apr 30, 2021

Authorized Representative

Name

QCS International LTD.

Relationship Type

UK Responsible Person

Address

Suite 9 Cumbernauld Business Park Wardpark Road

Cumbernauld, North Lanarkshire, Scotland, United Kingdom

Postcode: G67 3JZ

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Dermal tissue reconstructive material, synthetic mineral - UK MHRA Medical Device Registration

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