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Stimulite Contour

by Stimulite AB 31 variants

Part of a family of 166 devices: see the family page

Ref CD1314Model Contour

Stimulite Contour (CD1314) is a Class I device made by Stimulite AB, registered in EUDAMED on 23 Oct 2026 (Basic UDI-DI 073402472ContourGV), active as of 7 Nov 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number073402472ContourGV Basic UDI-DI 07340247299816UDI-DIDate23 Oct 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
CountourH
Model / reference
Contour, CD1314
Primary DI / UDI-DI
07340247299816
Basic UDI-DI
073402472ContourGV
EMDN code
V08030102 Non-active anti-decubitus medical cushions
Device class
Class I
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Standard device
EU market of registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000060003

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Properties

Other properties (14, all answered No)