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 - Pavis SPA

Address:

Via Rossini 11B 21020 Buguggiate VA

Milan

21020

Italy

Authorised Representative/ UK Responsible Person
Name: Dacey Ltd
Address:

Sanatorium Road Canton

Cardiff

South Glamorgan CF11 8DG

United Kingdom

Code/Term Type

Ankle/foot orthosis Ankle/foot orthosis Class I

Lumbar spine orthosis Lumbar spine orthosis Class I

Shoulder/elbow/wrist orthosis Shoulder/elbow/wrist orthosis Class I

Lumbosacral spine orthosis hernia support Lumbosacral spine orthosis hernia support Class I

Cervical spine collar reusable Cervical spine collar reusable Class I

Wrist/hand orthosis Wrist/hand orthosis Class I

Knee/ankle/foot orthosis Knee/ankle/foot orthosis Class I

Postsurgical brassiere non-antimicrobial Postsurgical brassiere non-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
Ankle/foot orthosis	Ankle/foot orthosis	Class I
Lumbar spine orthosis	Lumbar spine orthosis	Class I
Shoulder/elbow/wrist orthosis	Shoulder/elbow/wrist orthosis	Class I
Lumbosacral spine orthosis hernia support	Lumbosacral spine orthosis hernia support	Class I
Cervical spine collar reusable	Cervical spine collar reusable	Class I
Wrist/hand orthosis	Wrist/hand orthosis	Class I
Knee/ankle/foot orthosis	Knee/ankle/foot orthosis	Class I
Postsurgical brassiere non-antimicrobial	Postsurgical brassiere non-antimicrobial	Class I