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Πεδιο Υφασματινο Χειρουργειου 150X150 Διπλο

by Αντιγονη Πετροπουλου Και Σια Οε

Ref ΜΔ150Χ150Π/300Model ΠΕΔΙΟ ΥΦΑΣΜΑΤΙΝΟ ΧΕΙΡΟΥΡΓΕΙΟΥ 100X100

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 Number5207356000486U5 Basic UDI-DI 05207356000561UDI-DIDate13 May 2022RegisteredStatusActive

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  • Withdrawn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
Πεδιο Υφασματινο Χειρουργειου
Model / Reference
ΠΕΔΙΟ ΥΦΑΣΜΑΤΙΝΟ ΧΕΙΡΟΥΡΓΕΙΟΥ 100X100, ΜΔ150Χ150Π/300
Primary DI / UDI-DI
05207356000561
Basic UDI-DI
5207356000486U5
EMDN Code
T02010102 Incision drapes, with antibacterial agent
Device Class
Class I
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000019297

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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