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 - Royal Brompton & Harefield NHS Foundation Trust

Address:

Clinical Engineering Department Royal Brompton Hospital

Sydney Street

London

SW3 6NP

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

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

Surgical Procedure Packs (Includes Instruments Supplied Singularly) Surgical Procedure Packs (Includes Instruments Supplied Singularly)

Non-Invasive Drainage Devices And Accessories Non-Invasive Drainage Devices And 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
Surgical Instruments (Re-Usable And Non-Powered)	Surgical Instruments (Re-Usable And Non-Powered)	Class I
Surgical Procedure Packs (Includes Instruments Supplied Singularly)	Surgical Procedure Packs (Includes Instruments Supplied Singularly)
Non-Invasive Drainage Devices And Accessories	Non-Invasive Drainage Devices And Accessories	Class I