Corneal bur manual instrument - UK MHRA Medical Device Registration

Corneal bur manual instrument is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 114636. The device is manufactured by Bausch & Lomb GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Bausch & Lomb U.K. Ltd..

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Corneal bur manual instrument

MHRA Device ID: 114636•Ref: 114636

Device Type

General Medical Device

Devices

Corneal bur manual instrument

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 26, 2024

Manufacturer Information

Name

Bausch & Lomb GmbH

Address

Lilienthalstrasse 16, 18

Eppelheim, Germany

Created Date

Jul 2, 2021

Authorized Representative

Name

Bausch & Lomb U.K. Ltd.

Relationship Type

UK Responsible Person

Address

106-114 London Road

Kingston upon Thames, Surrey, England, United Kingdom

Postcode: KT2 6TN

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Corneal bur manual instrument - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Created Date

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DJ Fang

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