Corneoscleral punch - UK MHRA Medical Device Registration

Corneoscleral punch is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 103555. The device is manufactured by Moria S.A. from France, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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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Corneoscleral punch

MHRA Device ID: 103555•Ref: 103555

Device Type

General Medical Device

Devices

Corneoscleral punch

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Moria S.A.

Address

15 rue Georges Besse

Antony, France

Created Date

Aug 16, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Corneoscleral punch - UK MHRA Medical Device Registration

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