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 - PEMAX Kunststoff GmbH

Address:

Curiestraße 2

Stuttgart

70563

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

Medical equipment drape single-use Medical equipment drape 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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