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

Back to MHRA

Manufacturer's Devices - AMS Group Srl Soc. Unip.

Address:

Via Europa 12

San Pietro Viminario

Padova 35020

Italy

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

The Maltings East Tyndall Street Cardiff Bay

Cardiff

CF24 5EA

Wales United Kingdom

Code/Term Type

Endoscope sheath single-use Endoscope sheath single-use Class IIa

Analgesic PENS system probe single-use Analgesic PENS system probe single-use Class IIb

Analgesic PENS system Analgesic PENS system Class IIb

Analgesic PENS system Analgesic PENS system Class IIb

Contact details

Freedom of information

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

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Endoscope sheath single-use	Endoscope sheath single-use	Class IIa
Analgesic PENS system probe single-use	Analgesic PENS system probe single-use	Class IIb
Analgesic PENS system	Analgesic PENS system	Class IIb
Analgesic PENS system	Analgesic PENS system	Class IIb