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 - Medifactia AB

Address:

Medifactia AB C/O IOFFICE BUSINESS CENTER

Stockholm

11122

Sweden

Authorised Representative/ UK Responsible Person
Name: Mosaic Surgical LTD
Address:

9 York Way

High Wycombe

HP12 3PY

England United Kingdom

Code/Term Type

Flexible fibreoptic sinoscope Flexible fibreoptic sinoscope Class IIa

Imaging lesion localization marker ingestible Imaging lesion localization marker ingestible Class IIa

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
Flexible fibreoptic sinoscope	Flexible fibreoptic sinoscope	Class IIa
Imaging lesion localization marker ingestible	Imaging lesion localization marker ingestible	Class IIa