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 - Pronova Laboratories B.V.

Address:

Kruitpad 16

Muiden

1398 CP Muiden 1398

Netherlands

Authorised Representative/ UK Responsible Person
Name: World Foods Brand Management Ltd
Address:

98 Lancaster Road

Newcastle-u-Lyme

Newcastle-u-Lyme

Staffordshire ST5 1DS

England United Kingdom

Code/Term Type

Nasopharyngeal medicine administration kit Nasopharyngeal medicine administration kit Class I

Wart-removal cryogenic kit Wart-removal cryogenic kit Class IIa

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
Nasopharyngeal medicine administration kit	Nasopharyngeal medicine administration kit	Class I
Wart-removal cryogenic kit	Wart-removal cryogenic kit	Class IIa