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.B.M. s.r.l. Medical Equipment

Address:

Via Castello 10

Torre De' Picenardi

Cremona 26038

Italy

Authorised Representative/ UK Responsible Person
Name: QCS International LTD.
Address:

Suite 9 Cumbernauld Business Park

Wardpark Road

Cumbernauld

North Lanarkshire G67 3JZ

Scotland United Kingdom

Code/Term Type

Aerobic laboratory incubator Aerobic laboratory incubator Class I

Device sterilization/disinfection container reusable Device sterilization/disinfection container reusable Class I

Sterilization packaging single-use Sterilization packaging single-use Class I

Sterilization packaging reusable Sterilization packaging reusable 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
Aerobic laboratory incubator	Aerobic laboratory incubator	Class I
Device sterilization/disinfection container reusable	Device sterilization/disinfection container reusable	Class I
Sterilization packaging single-use	Sterilization packaging single-use	Class I
Sterilization packaging reusable	Sterilization packaging reusable	Class I