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Mi̇nör Cerrahi̇ Örtüsü 20(±10)X20(±10)Cm

by Bayteks Tekni̇k Teksti̇l San. Ve Ti̇c. A.Ş.

Ref 30100002384

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 Number86817441ST30100001421AB Basic UDI-DI 08681744100335UDI-DIDate12 May 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  • Withdrawn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

Device Name
Cerrahi̇ Örtü
Model / Reference
30100002384
Primary DI / UDI-DI
08681744100335
Basic UDI-DI
86817441ST30100001421AB
Direct Marketing DI
08681744100335
EMDN Code
T020102 Specialistic surgery drapes
Device Class
Class I
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000024488

Other devices from Bayteks Tekni̇k Teksti̇l San. Ve Ti̇c. A.Ş.

See all devices from Bayteks Tekni̇k Teksti̇l San. Ve Ti̇c. A.Ş. →

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