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 - Mego Afek AC Ltd

Address:

Kibbutz Afek

Afek

3004200

Israel

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

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Sequential venous compression system pump Sequential venous compression system pump Class IIa

Multi-chamber venous compression system garment reusable Multi-chamber venous compression system garment reusable Class IIa

Multi-chamber venous compression system garment single-use Multi-chamber venous compression system garment single-use Class IIa

Single-chamber venous compression system garment single-use Single-chamber venous compression system garment 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
Sequential venous compression system pump	Sequential venous compression system pump	Class IIa
Multi-chamber venous compression system garment reusable	Multi-chamber venous compression system garment reusable	Class IIa
Multi-chamber venous compression system garment single-use	Multi-chamber venous compression system garment single-use	Class IIa
Single-chamber venous compression system garment single-use	Single-chamber venous compression system garment single-use	Class IIa