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 - Micropos Medical AB

Address:

Adolf Edelsvärds gata 11

Göteborg

414 51

Sweden

Authorised Representative/ UK Responsible Person
Name: QAdvis UK Ltd
Address:

55-66 Frederick Street

Edinburgh EH2 1LS

EH2 1LS

Scotland United Kingdom

Code/Term Type

Radiation therapy lesion localization urethral catheter procedural Radiation therapy lesion localization urethral catheter procedural Class IIa

Radiation therapy lesion localization urethral catheter planning Radiation therapy lesion localization urethral catheter planning Class IIa

Radiation therapy invasive marker lesion localization system Radiation therapy invasive marker lesion localization system Class IIb

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
Radiation therapy lesion localization urethral catheter procedural	Radiation therapy lesion localization urethral catheter procedural	Class IIa
Radiation therapy lesion localization urethral catheter planning	Radiation therapy lesion localization urethral catheter planning	Class IIa
Radiation therapy invasive marker lesion localization system	Radiation therapy invasive marker lesion localization system	Class IIb