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 - Ascom UMS srl

Address:

Via Amilcare Ponchielli 29

Scandicci

50018

Italy

Authorised Representative/ UK Responsible Person
Name: Ascom (UK) LTD.
Address:

Wall Island Birmingham Rd

Lichfield

WS14 0QP

United Kingdom

Code/Term Type

Patient health record information system Patient health record information system Class IIb

Patient health record information system Patient health record information system 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
Patient health record information system	Patient health record information system	Class IIb
Patient health record information system	Patient health record information system	Class IIb