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 - Invivo Corporation

Address:

3545 SW 47th Avenue

Gainesville

Florida 32608

United States

Authorised Representative/ UK Responsible Person
Name: Philips Electronics UK Ltd
Address:

Ascent 1 Farnborough Aerospace Centre

Farnborough

Hampshire GU14 6XW

England United Kingdom

Code/Term Type

MRI system coil radio-frequency MRI system coil radio-frequency Class IIa

Needle guide single-use Needle guide single-use Class I

Needle guide single-use Needle guide single-use Class I

Needle guide single-use Needle guide single-use Class I

Needle guide single-use Needle guide single-use Class I

Needle guide single-use Needle guide single-use 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
MRI system coil radio-frequency	MRI system coil radio-frequency	Class IIa
Needle guide single-use	Needle guide single-use	Class I
Needle guide single-use	Needle guide single-use	Class I
Needle guide single-use	Needle guide single-use	Class I
Needle guide single-use	Needle guide single-use	Class I
Needle guide single-use	Needle guide single-use	Class IIa