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Urine Bag

by Zibo Eastmed Healthcare Products Co., Ltd.

Ref DMUB-P2000

Urine Bag (DMUB-P2000) is a Class I device made by Zibo Eastmed Healthcare Products Co., Ltd., registered in EUDAMED on 30 Jul 2026 (Basic UDI-DI B-6971077613975AK), active as of 25 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-6971077613975AK Basic UDI-DI Date30 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Urine Bag
Model / reference
DMUB-P2000
Primary DI / UDI-DI
D-6971077613975AK, D-69710776138419V
Basic UDI-DI
B-6971077613975AK, B-69710776138419V
EMDN code
A06030301, A03010101
Device class
Class I
EU registration type
Legacy device (under a directive)
EU market of registration
Latvia

Manufacturer details

EUDAMED SRN
CN-MF-000032259
Authorised representative
HUMISS TRADING S. L. ES-AR-000040177

Similar devices in this category

Other devices filed under INFUSION CONTROLLERS WITH OR W/O AIR INLET.

Other devices from Zibo Eastmed Healthcare Products Co., Ltd.

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Properties

  • Supplied sterile
  • Administering medicine
Other properties (10, all answered No)