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 - Medtronic Navigation Inc.

Address:

300 Foster Street

Littleton

MA 01460

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

Portable general-purpose fluoroscopic x-ray system digital Portable general-purpose fluoroscopic x-ray system digital Class IIb

Medical equipment drape single-use Medical equipment drape single-use Class I

Computer mouse/roller-ball Computer mouse/roller-ball Class I

Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system Class I

Multi-purpose stereotactic surgery system Multi-purpose stereotactic surgery system

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
Portable general-purpose fluoroscopic x-ray system digital	Portable general-purpose fluoroscopic x-ray system digital	Class IIb
Medical equipment drape single-use	Medical equipment drape single-use	Class I
Computer mouse/roller-ball	Computer mouse/roller-ball	Class I
Multi-purpose stereotactic surgery system	Multi-purpose stereotactic surgery system	Class I
Multi-purpose stereotactic surgery system	Multi-purpose stereotactic surgery system