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 - Ermis MedTech GmbH

Address:

Dornierstraße 49

Tuttlingen

78532

Germany

Authorised Representative/ UK Responsible Person
Name: MEDAGENT INTERNATIONAL UK LIMITED
Address:

2 St Andrews Place

Lewes

East Sussex BN7 1UP

England United Kingdom

Code/Term Type

Device sterilization/disinfection container reusable Device sterilization/disinfection container reusable Class I

Hamper Hamper Class I

Device sterilization/disinfection container single-use Device sterilization/disinfection container single-use 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
Device sterilization/disinfection container reusable	Device sterilization/disinfection container reusable	Class I
Hamper	Hamper	Class I
Device sterilization/disinfection container single-use	Device sterilization/disinfection container single-use	Class I
Device sterilization/disinfection container single-use	Device sterilization/disinfection container single-use	Class I