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.

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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

Name

Novomed Group

Address

12-14 rue Sarah Bernhardt

Asnieres-sur-Seine, France

Created Date

Jun 11, 2024

Authorized Representative

Name

Eurosurgical Ltd

Relationship Type

UK Responsible Person

Address

Merrow Business Park Guildford

Guildford, Surrey, England, United Kingdom

Postcode: GU4 7WA

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Other Products from Novomed Group (2)

Fixed-diameter cervical dilator, single-use

Type: General Medical Device

Registered: Nov 26, 2024

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Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

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

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