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 - CROMA PHARMA GmbH

Address:

Industriezeile 6

Leobendorf

2100

Austria

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

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

Vitreous/aqueous humour replacement medium intraoperative Vitreous/aqueous humour replacement medium intraoperative Class IIb

Lift thread bioabsorbable Lift thread bioabsorbable Class III

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

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 tissue reconstructive material microbe-derived	Dermal tissue reconstructive material microbe-derived	Class III
Vitreous/aqueous humour replacement medium intraoperative	Vitreous/aqueous humour replacement medium intraoperative	Class IIb
Lift thread bioabsorbable	Lift thread bioabsorbable	Class III
Dermal tissue reconstructive material microbe-derived anaesthetic	Dermal tissue reconstructive material microbe-derived anaesthetic	Class III