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Lágyrészvédő

by Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft. 23 variants

Ref 258900013

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5996527651DRLSLVNSTQF Basic UDI-DI 05996527011139UDI-DIDate19 Dec 2023RegisteredStatusActive

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  • Withdrawn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
Drill sleeve
Model / Reference
258900013
Primary DI / UDI-DI
05996527011139
Basic UDI-DI
5996527651DRLSLVNSTQF
EMDN Code
L0999 Orthopaedic and traumatological surgery instruments, reusable - other
Device Class
Class I
EU market of registration
Hungary

Manufacturer details

EUDAMED SRN
HU-MF-000006772

Other devices from Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft.

See all devices from Sanatmetal Ortopédiai és Traumatológiai Eszközöket Gyártó Kft. →

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