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Amniotic membrane perforator, reusable - UK MHRA Medical Device Registration

Amniotic membrane perforator, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 86057. The device is manufactured by DMS Holdings, Inc dba Healthsmart International, dba Briggs Medical from United States, classified as General Medical Device. The authorized representative in the UK is Medicare Colgate 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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Amniotic membrane perforator, reusable
MHRA Device ID: 86057โ€ขRef: 86057

Device Type

General Medical Device

Devices

Amniotic membrane perforator, reusable

Type

Class IIa

Date Registered

Jun 3, 2024

Last Updated

Apr 6, 2024

Manufacturer Information

Address

1931 Norman Drive

Waukegan, Illinois, United States

Created Date

Jun 22, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Unit 1/2 Post Cross Business Park

Cullompton, Devon, United Kingdom

Postcode: EX15 2BB

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