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 - bonyf AG

Address:

Heiligkreuz 16

Vaduz

FL-9490

Liechtenstein

Authorised Representative/ UK Responsible Person
Name: WHW Plastics Ltd
Address:

Therm Road Cleveland Street

Hull

North Humberside HU8 7BF

United Kingdom

Code/Term Type

Dental mouthwash Dental mouthwash Class I

Carboxymethylcellulose sodium/polymer denture adhesive zinc-free Carboxymethylcellulose sodium/polymer denture adhesive zinc-free Class I

Denture cleanser Denture cleanser Class I

Medical device disinfection agent Medical device disinfection agent Class IIb

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
Dental mouthwash	Dental mouthwash	Class I
Carboxymethylcellulose sodium/polymer denture adhesive zinc-free	Carboxymethylcellulose sodium/polymer denture adhesive zinc-free	Class I
Denture cleanser	Denture cleanser	Class I
Medical device disinfection agent	Medical device disinfection agent	Class IIb