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 - AMI INC.

Address:

#1412 SJ Techno Vile 278 Beotkkot-ro Geumcheon-gu Seoul Korea

Seoul

08511

South Korea

Authorised Representative/ UK Responsible Person
Name: CMC Medical Devices LTD
Address:

Office 32 19-21 Crawford Street

London

W1H 1PJ

United Kingdom

Code/Term Type

General/multiple surgical diode laser system General/multiple surgical diode laser system Class IIb

General/multiple surgical frequency-doubled solid-state laser system General/multiple surgical frequency-doubled solid-state laser system Class IIb

General/multiple surgical carbon dioxide laser system General/multiple surgical carbon dioxide laser system Class IIb

Intense pulsed light skin surface treatment system Intense pulsed light skin surface treatment system 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
General/multiple surgical diode laser system	General/multiple surgical diode laser system	Class IIb
General/multiple surgical frequency-doubled solid-state laser system	General/multiple surgical frequency-doubled solid-state laser system	Class IIb
General/multiple surgical carbon dioxide laser system	General/multiple surgical carbon dioxide laser system	Class IIb
Intense pulsed light skin surface treatment system	Intense pulsed light skin surface treatment system	Class IIa