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Bolsa de Orina

by Jiangsu Kangjin Medical Instrument Co., Ltd. 12 variants

Part of a family of 12 devices: see the family page

Ref TEST

Bolsa de Orina (TEST) is a Class I device made by Jiangsu Kangjin Medical Instrument Co., Ltd, registered in EUDAMED on 28 Apr 2026 (Basic UDI-DI 69419913UBHB), active as of 23 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69419913UBHB Basic UDI-DI 06942231699995UDI-DIDate28 Apr 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Collection Bag for Single Use
Model / reference
TEST
Primary DI / UDI-DI
06942231699995
Basic UDI-DI
69419913UBHB
EMDN code
A06030301 Urine collection bags
Device class
Class I
EU registration type
Standard device
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000011142
Authorised representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Similar devices in this category

Other devices filed under URINE COLLECTION BAGS.

Other devices from Jiangsu Kangjin Medical Instrument Co., Ltd

See all devices from Jiangsu Kangjin Medical Instrument Co., Ltd →

Properties

  • Supplied sterile
Other properties (13, all answered No)