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 - PLASMABIOTICS

Address:

116 Quai de Bezons

Argenteuil Cedex

95106

France

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

Unit D1 Heron Drive

Langley

Slough

Berks sl3 8pn

England United Kingdom

Code/Term Type

Endoscope clean-storage system Endoscope clean-storage system Class I

Luminal device flushing tubing set reusable Luminal device flushing tubing set reusable Class I

Device sterilization/disinfection container single-use Device sterilization/disinfection container 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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Code/Term		Type
Endoscope clean-storage system	Endoscope clean-storage system	Class I
Luminal device flushing tubing set reusable	Luminal device flushing tubing set reusable	Class I
Device sterilization/disinfection container single-use	Device sterilization/disinfection container single-use	Class I