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 - CLASSYS Inc.

Address:

CLASSYS 208 Teheran-ro Gangnam-gu

Seoul

06220

South Korea

Authorised Representative/ UK Responsible Person
Name: MT Promedt Consulting Ltd
Address:

Beaver House 23-38 Hythe Bridge Street

Oxford

OX1 2EP

England United Kingdom

Code/Term Type

Surgical/emergency suction cannula non-illuminating single-use Surgical/emergency suction cannula non-illuminating single-use Class I

Cryolipolysis body contouring system gel pad Cryolipolysis body contouring system gel pad Class I

Cryolipolysis body contouring system Cryolipolysis body contouring system Class IIa

Skin abrasion unit Skin abrasion unit Class IIa

Ultrasonic hyperthermia system Ultrasonic hyperthermia 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
Surgical/emergency suction cannula non-illuminating single-use	Surgical/emergency suction cannula non-illuminating single-use	Class I
Cryolipolysis body contouring system gel pad	Cryolipolysis body contouring system gel pad	Class I
Cryolipolysis body contouring system	Cryolipolysis body contouring system	Class IIa
Skin abrasion unit	Skin abrasion unit	Class IIa
Ultrasonic hyperthermia system	Ultrasonic hyperthermia system	Class IIa