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 - Resoundant Inc.

Address:

421 1st Avenue SW Suite 204W

Rochester

Minnesota 55902

United States

Authorised Representative/ UK Responsible Person
Name: AJW Technology Consulting Ltd
Address:

4/4a Bloomsbury Square

London

WC1A 2RP

England United Kingdom

Code/Term Type

Magnetic resonance elastography acoustic driver Magnetic resonance elastography acoustic driver Class IIa

MRI phantom test object MRI phantom test object Class I

MRI system application software MRI system application software 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
Magnetic resonance elastography acoustic driver	Magnetic resonance elastography acoustic driver	Class IIa
MRI phantom test object	MRI phantom test object	Class I
MRI system application software	MRI system application software	Class IIa