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 196770. The device is manufactured by RI.MOS srl from Italy, 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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Amniotic membrane perforator, single-use

MHRA Device ID: 196770•Ref: 196770

Device Type

General Medical Device

Devices

Amniotic membrane perforator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 11, 2024

Manufacturer Information

Name

RI.MOS srl

Address

Via Manuzio 15

Mirandola, Italy

Created Date

Jul 8, 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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Amniotic membrane perforator, single-use - UK MHRA Medical Device Registration

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Date Registered

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