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 - Avery Dennison Medical Ltd

Address:

IDA Business Park Ballinalee Road

Longford

N39 DX73

Ireland

Authorised Representative/ UK Responsible Person
Name: Psephos Limited
Address:

Sussex Innovation Centre Science Park Square

Falmer

Brighton

East Sussex BN1 9SB

England United Kingdom

Code/Term Type

Dry skin moisture barrier dressing Dry skin moisture barrier dressing Class I

Synthetic-polymer liquid barrier dressing Synthetic-polymer liquid barrier dressing Class I

Peristomal/periwound dressing Peristomal/periwound dressing Class I

Synthetic-polymer liquid barrier dressing sterile Synthetic-polymer liquid barrier dressing sterile 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
Dry skin moisture barrier dressing	Dry skin moisture barrier dressing	Class I
Synthetic-polymer liquid barrier dressing	Synthetic-polymer liquid barrier dressing	Class I
Peristomal/periwound dressing	Peristomal/periwound dressing	Class I
Synthetic-polymer liquid barrier dressing sterile	Synthetic-polymer liquid barrier dressing sterile	Class IIa