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Benda Di Ovatta Agugliata 20x300cm - 1 Involucro Sterile

by Tre A S.r.l.

Ref COD F30008Model Ovatta per ortopedia sterile

Active European Union

CE MDR

Valid until

2 Sep 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8032532361CODF3RW Basic UDI-DI 08032532360552UDI-DIDate16 Sep 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030215-00 Active

    Quality assurance EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    3 Sep 2026
    Expires
    2 Sep 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Benda di ovatta agugliata sterile
Model / Reference
Ovatta per ortopedia sterile, COD F30008
Primary DI / UDI-DI
08032532360552
Basic UDI-DI
8032532361CODF3RW
EMDN Code
M010299 Orthopaedic wadding - other
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000050860

Other devices from Tre A S.r.l.

See all devices from Tre A S.r.l. →

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