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 - Crown Aesthetics

Address:

5005 Lyndon B. Johnson Fwy Suite 370

Dallas

Texas 75244

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

General surgical procedure kit non-medicated single-use General surgical procedure kit non-medicated single-use Class IIa

Cosmetic micro-needling electronic handpiece cartridge professional Cosmetic micro-needling electronic handpiece cartridge professional Class IIa

Cosmetic micro-needling electronic handpiece professional Cosmetic micro-needling electronic handpiece professional Class IIa

Wound hydrogel dressing non-antimicrobial Wound hydrogel dressing non-antimicrobial 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 surgical procedure kit non-medicated single-use	General surgical procedure kit non-medicated single-use	Class IIa
Cosmetic micro-needling electronic handpiece cartridge professional	Cosmetic micro-needling electronic handpiece cartridge professional	Class IIa
Cosmetic micro-needling electronic handpiece professional	Cosmetic micro-needling electronic handpiece professional	Class IIa
Wound hydrogel dressing non-antimicrobial	Wound hydrogel dressing non-antimicrobial	Class IIa