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

Back to MHRA

Manufacturer's Devices - Apyx Medical Corporation

Address:

5115 Ulmerton Road

Clearwater

Florida 33760

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Electrosurgical handpiece single-use Electrosurgical handpiece single-use Class IIb

Electrosurgical system generator Electrosurgical system generator Class IIb

Electrosurgical return electrode single-use Electrosurgical return electrode single-use Class I

Foot-switch electrical Foot-switch electrical Class IIb

Calibration gas cylinder regulator Calibration gas cylinder regulator Class IIb

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Electrosurgical handpiece single-use	Electrosurgical handpiece single-use	Class IIb
Electrosurgical system generator	Electrosurgical system generator	Class IIb
Electrosurgical return electrode single-use	Electrosurgical return electrode single-use	Class I
Foot-switch electrical	Foot-switch electrical	Class IIb
Calibration gas cylinder regulator	Calibration gas cylinder regulator	Class IIb