Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Peregrine Surgical Ltd.

Address:

51 Britain Drive

New Britain

Pennsylvania 18901

United States

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Ophthalmic fibreoptic light instrument single-use Ophthalmic fibreoptic light instrument single-use Class IIa

Ophthalmic laser system beam guide Ophthalmic laser system beam guide Class IIa

Epiretinal/inner limiting membrane scraper single-use Epiretinal/inner limiting membrane scraper single-use Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Ophthalmic fibreoptic light instrument single-use	Ophthalmic fibreoptic light instrument single-use	Class IIa
Ophthalmic laser system beam guide	Ophthalmic laser system beam guide	Class IIa
Epiretinal/inner limiting membrane scraper single-use	Epiretinal/inner limiting membrane scraper single-use	Class IIa