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Practic

by Μπινης Ανωνυμος Εισαγωγικη Και Εμπορικη Εταιρεια Οικιακων Ειδων 54 variants

Ref 0-21013

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 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5203399glovesY3 Basic UDI-DI 05203399210370UDI-DIDate14 Apr 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  • Withdrawn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
Examination Gloves
Model / Reference
0-21013
Primary DI / UDI-DI
05203399210370
Basic UDI-DI
5203399glovesY3
EMDN Code
T010201 Latex examination / treatment gloves
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000018291

Other devices from Μπινης Ανωνυμος Εισαγωγικη Και Εμπορικη Εταιρεια Οικιακων Ειδων

See all devices from Μπινης Ανωνυμος Εισαγωγικη Και Εμπορικη Εταιρεια Οικιακων Ειδων →

Properties

  • Contains Latex

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Reusable: 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