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 - Surgical Instruments Group Holdings Ltd

Address:

Sovereign Court 230 Upper Fifth Street

Central Milton Keynes

Milton Keynes

Bucks MK9 2HR

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Device sterilization/disinfection container reusable Device sterilization/disinfection container reusable

Endoscope transport/sterilization protective cover reusable Endoscope transport/sterilization protective cover reusable Class I

Endoscope transport/sterilization protective cover reusable Endoscope transport/sterilization protective cover 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
Device sterilization/disinfection container reusable	Device sterilization/disinfection container reusable
Endoscope transport/sterilization protective cover reusable	Endoscope transport/sterilization protective cover reusable	Class I
Endoscope transport/sterilization protective cover reusable	Endoscope transport/sterilization protective cover reusable	Class I