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 - Valmed S.r.l.

Address:

Via dell'Industria 3

Tovo di Sant'Agata

Sondrio 23030

Italy

Authorised Representative/ UK Responsible Person
Name: Cyberpan Support Services Ltd
Address:

The Union Suite The Union Building

51-59 Rose Lane

Norwich

Norfolk NR1 1BY

England United Kingdom

Code/Term Type

Intravenous administration bag/bottle Intravenous administration bag/bottle Class IIa

Medication transfer set Medication transfer set 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
Intravenous administration bag/bottle	Intravenous administration bag/bottle	Class IIa
Medication transfer set	Medication transfer set	Class IIa