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 - Rhythmlink International LLC

Address:

1140 First Street South

Columbia

South Carolina 29209

United States

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Diagnostic peripheral nerve electrical stimulation system Diagnostic peripheral nerve electrical stimulation system Class IIa

Subdermal needle electrode Subdermal needle electrode Class IIa

Analytical scalp electrode single-use Analytical scalp electrode single-use 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
Diagnostic peripheral nerve electrical stimulation system	Diagnostic peripheral nerve electrical stimulation system	Class IIa
Subdermal needle electrode	Subdermal needle electrode	Class IIa
Analytical scalp electrode single-use	Analytical scalp electrode single-use	Class I