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Burr

by CIZETA SURGICAL S.r.l. 97 variants

Ref 04LA1242

Active European Union

CE MDR

Valid until

14 Sep 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier ITALCERT SRL

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 Number805004697P0180WQ Basic UDI-DI 08050046977554UDI-DIDate23 Oct 2023RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 029-00-00-MDR Active

    Quality management system EU MDR

    Certifier
    ITALCERT SRL 0426
    Issued
    15 Sep 2023
    Expires
    14 Sep 2028

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Burr
Model / Reference
04LA1242
Primary DI / UDI-DI
08050046977554
Basic UDI-DI
805004697P0180WQ
EMDN Code
P0180 Facial and odontological prostheses - accessories
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027906

Other devices from CIZETA SURGICAL S.r.l.

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    Class IIb

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    Class IIa

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    Class IIb

  • Pin Di Fissaggio

    Class IIb

  • Burr

    Class IIa

  • Burr

    Class IIa

See all devices from CIZETA SURGICAL S.r.l. →

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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