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Vomit Bag

by Curas Sdn. Bhd. 4 variants

Ref 03052

Vomit Bag (03052) is a Class I device made by Curas Sdn. Bhd., registered in EUDAMED on 20 Apr 2026 (Basic UDI-DI 5051400VBG01XXXXX9Z), 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 Number5051400VBG01XXXXX9Z Basic UDI-DI 05051400030529UDI-DIDate20 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  • Withdrawn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
Vomit Bag
Model / reference
03052
Primary DI / UDI-DI
05051400030529
Basic UDI-DI
5051400VBG01XXXXX9Z
EMDN code
A0699 Drainage and fluid collection devices - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Poland

Manufacturer details

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

Similar devices in this category

Other devices filed under DRAINAGE AND FLUID COLLECTION DEVICES - OTHER.

Other devices from Curas Sdn. Bhd.

See all devices from Curas Sdn. Bhd. →

Properties

Other properties (14, all answered No)