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 - Therenva SAS

Address:

74F rue de Paris

Rennes

35000

France

Authorised Representative/ UK Responsible Person
Name: Xograph Healthcare limited
Address:

Xograph House Ebley Road

Stonehouse

Gloucestershire GL10 2LU

United Kingdom

Code/Term Type

Radiology DICOM image processing application software Radiology DICOM image processing application software Class IIa

Surgical planning/navigation-enhancement system Surgical planning/navigation-enhancement system 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
Radiology DICOM image processing application software	Radiology DICOM image processing application software	Class IIa
Surgical planning/navigation-enhancement system	Surgical planning/navigation-enhancement system	Class I