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Tappo in polietilene con gancio per urinali uomo in sacchetto COMED

by Syntesys S.R.L.

Ref 16 200 22BModel Urinale in plastica

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805414149URINALES5 Basic UDI-DI 08054141493131UDI-DIDate11 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  • Withdrawn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
Urinale in plastica
Model / Reference
Urinale in plastica, 16 200 22B
Primary DI / UDI-DI
08054141493131
Basic UDI-DI
805414149URINALES5
EMDN Code
V0812, Y091299
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
IT-MF-000027856

From the manufacturer

Manufacturer's product page: Anatomia patologica Per un’area di diagnostica consolidata offriamo prodotti garantiti e di qualità confermata.

Other devices from Syntesys S.R.L.

See all devices from Syntesys S.R.L. →

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