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 - Dermoaroma Italy Srl

Address:

Dermoaroma Italy Srl Via dei Pirenei 1

Rome

00144

Italy

Authorised Representative/ UK Responsible Person
Name: D-BIOTECH LTD
Address:

24 West Road

Stanley

DH9 8HU

England United Kingdom

Code/Term Type

Haematological concentrate system preparation kit platelet concentration Haematological concentrate system preparation kit platelet concentration Class IIa

Deep skin exfoliant Deep skin exfoliant Class IIb

Dermal tissue reconstructive material microbe-derived Dermal tissue reconstructive material microbe-derived Class III

Nitrile examination/treatment glove non-powdered non-antimicrobial Nitrile examination/treatment glove non-powdered non-antimicrobial Class I

Autologous blood collection tube Autologous blood collection tube 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
Haematological concentrate system preparation kit platelet concentration	Haematological concentrate system preparation kit platelet concentration	Class IIa
Deep skin exfoliant	Deep skin exfoliant	Class IIb
Dermal tissue reconstructive material microbe-derived	Dermal tissue reconstructive material microbe-derived	Class III
Nitrile examination/treatment glove non-powdered non-antimicrobial	Nitrile examination/treatment glove non-powdered non-antimicrobial	Class I
Autologous blood collection tube	Autologous blood collection tube	Class IIa