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Amniotic membrane perforator, single-use - UK MHRA Medical Device Registration

Amniotic membrane perforator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195161. The device is manufactured by Novomed Group from France, classified as General Medical Device. The authorized representative in the UK is Eurosurgical 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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General Medical Device
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Amniotic membrane perforator, single-use
MHRA Device ID: 195161•Ref: 195161

Device Type

General Medical Device

Devices

Amniotic membrane perforator, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Address

12-14 rue Sarah Bernhardt

Asnieres-sur-Seine, France

Created Date

Jun 11, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

Merrow Business Park Guildford

Guildford, Surrey, England, United Kingdom

Postcode: GU4 7WA

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