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 - New Pelvic Pain Technologies Inc.

Address:

548 Market Street Suite 88577

San Francisco

California 94104

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

External manual massager clinical External manual massager clinical Class I

Hand-held electric massager Hand-held electric massager Class I

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
External manual massager clinical	External manual massager clinical	Class I
Hand-held electric massager	Hand-held electric massager	Class I