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Silicone Reservoir

by Jiangsu Yangtze River Medical Technology Corp. 5 variants

Ref 01.9082Model 100ml、200ml、400ml

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69237643AYCEFYQXZ Basic UDI-DI 06923764329832UDI-DIDate25 Aug 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
100ml、200ml、400ml, 01.9082
Primary DI / UDI-DI
06923764329832
Basic UDI-DI
69237643AYCEFYQXZ
EMDN Code
A060301 Collection bags and other containers for drainages and fistulas, single use
Device Class
Class I
EU market of registration
Cyprus

Manufacturer details

EUDAMED SRN
CN-MF-000027308
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Jiangsu Yangtze River Medical Technology Corp.

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Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No