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 - Smart Medical Systems Ltd

Address:

5 HaNofar Street

Raanana

4366404

Israel

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

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Flexible video upper/lower gastrointestinal endoscope Flexible video upper/lower gastrointestinal endoscope Class IIa

Endoscopic overtube single-use Endoscopic overtube single-use Class IIa

Catheter/overtube balloon inflator reusable Catheter/overtube balloon inflator reusable Class I

Invasive medical device leak tester electrical Invasive medical device leak tester electrical Class I

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
Flexible video upper/lower gastrointestinal endoscope	Flexible video upper/lower gastrointestinal endoscope	Class IIa
Endoscopic overtube single-use	Endoscopic overtube single-use	Class IIa
Catheter/overtube balloon inflator reusable	Catheter/overtube balloon inflator reusable	Class I
Invasive medical device leak tester electrical	Invasive medical device leak tester electrical	Class I