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 - Laminate Medical Technologies Ltd

Address:

24 Raoul Wallenberg Street

Tel Aviv

6971921

Israel

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

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Open-surgery blood vessel sizer single-use Open-surgery blood vessel sizer single-use Class IIa

Arteriovenous fistula extraluminal mesh-sleeve Arteriovenous fistula extraluminal mesh-sleeve Class IIb

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
Open-surgery blood vessel sizer single-use	Open-surgery blood vessel sizer single-use	Class IIa
Arteriovenous fistula extraluminal mesh-sleeve	Arteriovenous fistula extraluminal mesh-sleeve	Class IIb