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 - Danumed Medizintechnik GmbH

Address:

Stadtamhof 18

Regensburg

93059

Germany

Authorised Representative/ UK Responsible Person
Name: Psephos Limited
Address:

Sussex Innovation Centre Science Park Square

Falmer

Brighton

East Sussex BN1 9SB

England United Kingdom

Code/Term Type

Gastrostomy button Gastrostomy button

Gastrostomy tube Gastrostomy tube

Enteral tube extension Enteral tube extension

Enteral tube extension non-sterile Enteral tube extension non-sterile

Gastrostomy depth sizer Gastrostomy depth sizer 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
Gastrostomy button	Gastrostomy button
Gastrostomy tube	Gastrostomy tube
Enteral tube extension	Enteral tube extension
Enteral tube extension non-sterile	Enteral tube extension non-sterile
Gastrostomy depth sizer	Gastrostomy depth sizer	Class I