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 - C.I.O.M. SRL

Address:

VIA SAPRI 14/6

Milan

20156 MILANO

Italy

Authorised Representative/ UK Responsible Person
Name: Bakers Instrument Brokers Ltd. T/A BIB Ophthalmic Instruments
Address:

Unit 8 The Orbital Centre Cockerel Close

Stevenage

Hertfordshire SG1 2NB

United Kingdom

Code/Term Type

Trial lens set Trial lens set Class I

Trial lens frame Trial lens frame 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
Trial lens set	Trial lens set	Class I
Trial lens frame	Trial lens frame	Class I