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 - Aesthetic Group

Address:

ZAC de La Gobette

Puiseux Le Hauberger

60540

France

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

Dermal curette Dermal curette Class IIa

Skin-coring punch single-use Skin-coring punch single-use Class IIa

Liposuction system cannula single-use Liposuction system cannula single-use Class IIa

Tissue injection cannula Tissue injection cannula 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 curette	Dermal curette	Class IIa
Skin-coring punch single-use	Skin-coring punch single-use	Class IIa
Liposuction system cannula single-use	Liposuction system cannula single-use	Class IIa
Tissue injection cannula	Tissue injection cannula	Class IIa