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 - CANNORDIC A/S

Address:

Fruebjergvej 3

Copenhagen

DK-2100

Denmark

Authorised Representative/ UK Responsible Person
Name: AF PHARMA SERVICE UK LTD
Address:

Suite 140 Temple Chambers 3-7 Temple Avenue

London

EC4Y 0DA

England United Kingdom

Code/Term Type

Nasal mucosa dressing non-antimicrobial Nasal mucosa dressing non-antimicrobial Class I

Cold/cool therapy gel Cold/cool therapy gel Class I

Nasal mucosa infection control gel Nasal mucosa infection control gel Class I

Inflammatory skin/nerve/joint disorder dressing Inflammatory skin/nerve/joint disorder dressing Class I

Wound hydrogel dressing antimicrobial Wound hydrogel dressing antimicrobial 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
Nasal mucosa dressing non-antimicrobial	Nasal mucosa dressing non-antimicrobial	Class I
Cold/cool therapy gel	Cold/cool therapy gel	Class I
Nasal mucosa infection control gel	Nasal mucosa infection control gel	Class I
Inflammatory skin/nerve/joint disorder dressing	Inflammatory skin/nerve/joint disorder dressing	Class I
Wound hydrogel dressing antimicrobial	Wound hydrogel dressing antimicrobial	Class I