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 - CODAN ARGUS AG

Address:

Oberneuhofstrasse 10

Baar

CH-6340

Switzerland

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

1 Eastheath Avenue

Wokingham

Berkshire RG41 2PR

England United Kingdom

Code/Term Type

Bedside infusion pump single-channel Bedside infusion pump single-channel Class IIb

Bedside syringe pump Bedside syringe pump Class IIb

Infusion pump management unit mobile Infusion pump management unit mobile 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
Bedside infusion pump single-channel	Bedside infusion pump single-channel	Class IIb
Bedside syringe pump	Bedside syringe pump	Class IIb
Infusion pump management unit mobile	Infusion pump management unit mobile	Class I