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SAP by Curas™

by Curas Sdn. Bhd. 4 variants

Ref 09602

SAP by Curas™ (09602) is a Class I device made by Curas Sdn. Bhd., registered in EUDAMED on 23 Apr 2026 (Basic UDI-DI 5051400SAP01PADXXYW), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5051400SAP01PADXXYW Basic UDI-DI 05051400096020UDI-DIDate23 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  • Withdrawn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
SAP by Curas™
Model / reference
09602
Primary DI / UDI-DI
05051400096020
Basic UDI-DI
5051400SAP01PADXXYW
EMDN code
T0499 Incontinence devices - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

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

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Other devices filed under INCONTINENCE DEVICES - OTHER.

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Properties

Other properties (14, all answered No)