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 - Medicom Healthcare BV

Address:

Parallelweg 80a

3931 MT Woudenberg

NA

Netherlands

Authorised Representative/ UK Responsible Person
Name: Medicom HealthPro Limited
Address:

Unit 1 Liliput Close

Northampton

United Kingdom NN4 7EJ

United Kingdom

Code/Term Type

Sterilization packaging single-use Sterilization packaging 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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