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 - NTC Srl

Address:

Via L. Razza 3

Milan

Lombardy Region 20124

Italy

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

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Corneal oedema solution/ointment Corneal oedema solution/ointment Class IIa

Intestinal mucosa barrier Intestinal mucosa barrier Class IIa

Eye lubricant Eye lubricant Class IIa

Dry powder inhaler Dry powder inhaler Class IIa

Dry powder inhaler Dry powder inhaler Class IIa

Dry powder inhaler Dry powder inhaler Class IIa

Dry powder inhaler Dry powder inhaler Class I

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
Corneal oedema solution/ointment	Corneal oedema solution/ointment	Class IIa
Intestinal mucosa barrier	Intestinal mucosa barrier	Class IIa
Eye lubricant	Eye lubricant	Class IIa
Dry powder inhaler	Dry powder inhaler	Class IIa
Dry powder inhaler	Dry powder inhaler	Class IIa
Dry powder inhaler	Dry powder inhaler	Class IIa
Dry powder inhaler	Dry powder inhaler	Class I