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Male Urinal

by Jinhua Feng Chuang Technology Co., Ltd.

Ref SA7243005Model SA7243005,PC23201-M-6, 2311,2295,3005,3006,3006-1, 1003,1004,2041,2042,2044

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697992447MU001TK Basic UDI-DI 06979924470012UDI-DIDate30 Mar 2026RegisteredStatusActive

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  • Withdrawn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
Male Urinal
Model / Reference
SA7243005, PC23201-M-6, 2311, 2295, 3005, 3006, 3006-1, 1003, 1004, 2041, 2042, 2044
Primary DI / UDI-DI
06979924470012
Basic UDI-DI
697992447MU001TK
EMDN Code
V0812 Feces and urine collection aids (bed pans and parrots)
Device Class
Class I
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
CN-MF-000052632
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Jinhua Feng Chuang Technology Co., Ltd.

Properties

Other properties (13)

  • Sterile: No
  • 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