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 - Ampcare LLC

Address:

1120 South Freeway Suite 111

Fort Worth

Texas 76104

United States

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Cervicothoracic spine orthosis Cervicothoracic spine orthosis Class I

Transcutaneous electrical stimulation lead Transcutaneous electrical stimulation lead Class I

Transcutaneous electrical stimulation electrode single-use Transcutaneous electrical stimulation electrode single-use Conformity Assessment Certificate Expired Class IIa

Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Conformity Assessment Certificate Expired 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
Cervicothoracic spine orthosis	Cervicothoracic spine orthosis	Class I
Transcutaneous electrical stimulation lead	Transcutaneous electrical stimulation lead	Class I
Transcutaneous electrical stimulation electrode single-use	Transcutaneous electrical stimulation electrode single-use Conformity Assessment Certificate Expired	Class IIa
Physical therapy transcutaneous neuromuscular electrical stimulation system	Physical therapy transcutaneous neuromuscular electrical stimulation system Conformity Assessment Certificate Expired	Class IIa