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 - Wipak Oy

Address:

Wipaktie 2

Nastola

15560

Finland

Authorised Representative/ UK Responsible Person
Name: Wipak UK Ltd.
Address:

3 Buttington Business Park Welshpool

SY21 8SL Welshpool

Welshpool

Powys SY21 8SL

Wales 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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