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 - Cytophil Inc.

Address:

2485 Corporate Circle Suite 2

East Troy

WI 53120

United States

Authorised Representative/ UK Responsible Person
Name: QCS International LTD.
Address:

Suite 9 Cumbernauld Business Park

Wardpark Road

Cumbernauld

North Lanarkshire G67 3JZ

Scotland United Kingdom

Code/Term Type

Dermal tissue reconstructive material synthetic mineral Dermal tissue reconstructive material synthetic mineral Class III

Injectable vocal cord medialization implant synthetic Injectable vocal cord medialization implant synthetic Class III

General-purpose endoscopic needle single-use General-purpose endoscopic needle 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
Dermal tissue reconstructive material synthetic mineral	Dermal tissue reconstructive material synthetic mineral	Class III
Injectable vocal cord medialization implant synthetic	Injectable vocal cord medialization implant synthetic	Class III
General-purpose endoscopic needle single-use	General-purpose endoscopic needle single-use	Class IIa