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 - BOLSAPLAST

Address:

C. Bernat Metge 110-112

Sabadell

08205

Spain

Authorised Representative/ UK Responsible Person
Name: RQMIS AR Ltd.
Address:

4 Whitan Way

Witney

OX28 6FF

England United Kingdom

Code/Term Type

Sterilization packaging single-use Sterilization packaging single-use 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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