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 90992. The device is manufactured by Peregrine Surgical, LLC from United States, classified as General Medical Device. The authorized representative in the UK is Advena 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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Epiretinal/inner limiting membrane scraper, single-use

MHRA Device ID: 90992•Ref: 90992

Device Type

General Medical Device

Devices

Epiretinal/inner limiting membrane scraper, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 12, 2024

Manufacturer Information

Name

Peregrine Surgical, LLC

Address

51 Britain Drive

New Britain, Pennsylvania, United States

Created Date

Jul 29, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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

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