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 - AiBiomed Corp

Address:

114 E. Haley St.

Santa Barbara

CA 93101-5323

United States

Authorised Representative/ UK Responsible Person
Name: Medtronic Limited
Address:

Building 9 Croxley Park

Watford

Herts WD18 8WW

England United Kingdom

Code/Term Type

Intraoperative parathyroid detection system probe Intraoperative parathyroid detection system probe Class IIa

Intraoperative parathyroid detection system probe Intraoperative parathyroid detection system probe 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
Intraoperative parathyroid detection system probe	Intraoperative parathyroid detection system probe	Class IIa
Intraoperative parathyroid detection system probe	Intraoperative parathyroid detection system probe	Class IIa