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Telo Ortopedia per Isolamento Verticale Cm 240X320 Con Incision Film in Pe Trasparente - Sterile

by Mediberg S.r.l. Unipersonale 4 variants

Ref 101017FDCSME

Active European Union

CE MDR

Valid until

5 Aug 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ICIM S.P.A.

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 Number0425-MDR-030213-00 Date6 Aug 2026IssuedStatusActive expires 5 Aug 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030213-00 Active

    Quality assurance EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    6 Aug 2026
    Expires
    5 Aug 2031

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Telo Chirurgico Sterile
Model / Reference
101017FDCSME
Primary DI / UDI-DI
08030413020106
Basic UDI-DI
8030413FTS02NR
EMDN Code
T020102 Specialistic surgery drapes
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000012712

Other devices from Mediberg S.r.l. Unipersonale

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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