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Human Waste Collection

by Curas Sdn. Bhd. 4 variants

Ref 08009, 08602, 08040, 09094, 08000, 08603, 08034, 08001, 09093

Human Waste Collection (08009) is a Class I device made by Curas Sdn. Bhd., registered in EUDAMED on 20 Apr 2026 (Basic UDI-DI 5051400BSP01XXXXX9F), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5051400BSP01XXXXX9F Basic UDI-DI Date20 Apr 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  • Withdrawn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
Human Waste Collection
Model / reference
08009, 08602, 08040, 09094, 08000, 08603, 08034, 08001, 09093
Primary DI / UDI-DI
05051400080098, 05051400086021, 05051400080401, 05051400090943, 05051400080005, 05051400086038, 05051400080340, 05051400080012, 05051400090936
Basic UDI-DI
5051400BSP01XXXXX9F, 5051400USM01XXXXXQV, 5051400JUG01XXXXXCS
EMDN code
V0499, V0401, V0480
Device class
Class I
EU registration type
Standard device
EU market of registration
Ireland
Netherlands
Denmark
Austria

Manufacturer details

EUDAMED SRN
MY-MF-000036883
Authorised representative
Kabomed GmbH AT-AR-000007569

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Properties

Other properties (14, all answered No)