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 - BETATEX S.p.a

Address:

VIA RAFFAELLO 2

ASSISI

Perugia 06081

Italy

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

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

General surgical procedure kit non-medicated single-use General surgical procedure kit non-medicated single-use Class IIa

Ophthalmic surgical drape Ophthalmic surgical drape Class IIa

Patient surgical drape single-use Patient surgical drape 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
General surgical procedure kit non-medicated single-use	General surgical procedure kit non-medicated single-use	Class IIa
Ophthalmic surgical drape	Ophthalmic surgical drape	Class IIa
Patient surgical drape single-use	Patient surgical drape single-use	Class IIa