Epiretinal/inner limiting membrane scraper, single-use - UK MHRA Medical Device Registration

Epiretinal/inner limiting membrane scraper, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 168971. The device is manufactured by Alcon Laboratories, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Alcon Eye Care UK Limited.

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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Epiretinal/inner limiting membrane scraper, single-use

MHRA Device ID: 168971•Ref: 168971

Device Type

General Medical Device

Devices

Epiretinal/inner limiting membrane scraper, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 23, 2024

Manufacturer Information

Name

Alcon Laboratories, Inc.

Address

6201 South Freeway

Fort Worth, United States

Created Date

Apr 27, 2021

Authorized Representative

Name

Alcon Eye Care UK Limited

Relationship Type

UK Responsible Person

Address

Park View, Riverside Way Watchmoor Park

Camberley, Surrey, United Kingdom

Postcode: GU15 3YL

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Epiretinal/inner limiting membrane scraper, single-use - UK MHRA Medical Device Registration

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