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 - Kohlbrat & Bunz Gesellschaft m.b.H

Address:

Loretostr 6-8

Radstad

5550

Austria

Authorised Representative/ UK Responsible Person
Name: Medical Device Management Ltd
Address:

31 Braintree Business Park Blackwell Drive

Braintree

Essex CM7 2PU

England United Kingdom

Code/Term Type

Patient positioning vacuum mattress Patient positioning vacuum mattress Class I

Vacuum mouldable splint Vacuum mouldable splint Class I

Limb/torso/head restraint reusable Limb/torso/head restraint reusable Class I

Head/neck immobilizer reusable Head/neck immobilizer reusable 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
Patient positioning vacuum mattress	Patient positioning vacuum mattress	Class I
Vacuum mouldable splint	Vacuum mouldable splint	Class I
Limb/torso/head restraint reusable	Limb/torso/head restraint reusable	Class I
Head/neck immobilizer reusable	Head/neck immobilizer reusable	Class I