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 - The National Artificial Eye Service

Address:

221 Bristol Avenue

Blackpool

Lancashire FY2 0BF

United Kingdom

Authorised Representative/ UK Responsible Person
Name:
Address:

Code/Term Type

Artificial Eyes Class I

Surgical Instruments (Re-Usable And Non-Powered) Class I

Dental Prophylaxis Paste (Non-Fluoride) Class I

Contact Lens accessories 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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Code/Term		Type
Artificial Eyes		Class I
Surgical Instruments (Re-Usable And Non-Powered)		Class I
Dental Prophylaxis Paste (Non-Fluoride)		Class I
Contact Lens accessories		Class I