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 - Acto GmbH

Address:

Schulstrasse 8

Schulstr. Wietzen

Nienburg (Weser)

Hannover 31613

Germany

Authorised Representative/ UK Responsible Person
Name: Creed Medical Ltd
Address:

Synergy House Commercial Gate

Mansfield

Nottinghamshire NG18 1EX

England United Kingdom

Code/Term Type

Antimicrobial wound irrigation solution Antimicrobial wound irrigation solution Class III

Wound hydrogel dressing antimicrobial Wound hydrogel dressing antimicrobial Class III

Organic peroxy acid device sterilant single-use Organic peroxy acid device sterilant single-use Class IIb

Medical device disinfection agent Medical device disinfection agent Class IIb

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
Antimicrobial wound irrigation solution	Antimicrobial wound irrigation solution	Class III
Wound hydrogel dressing antimicrobial	Wound hydrogel dressing antimicrobial	Class III
Organic peroxy acid device sterilant single-use	Organic peroxy acid device sterilant single-use	Class IIb
Medical device disinfection agent	Medical device disinfection agent	Class IIb