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Leva per radici punta piatta # 3BFT Bein 3mm

by Lascod S.P.A. (Laboratori Scientifici Odontoiatria)

Ref ZFT082

Active European Union

CE MDR

Valid until

1 Oct 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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0425-MDR-030227-00 Date2 Oct 2026IssuedStatusActive expires 1 Oct 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 0425-MDR-030227-00 Active

    Quality assurance EU MDR

    Certifier
    ICIM S.P.A. 0425
    Issued
    2 Oct 2026
    Expires
    1 Oct 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Strumentario Chirurgico Riutilizzabile
Model / Reference
ZFT082
Primary DI / UDI-DI
18016200520742
Basic UDI-DI
8016200DESCRI001RM
EMDN Code
L159099 Odontostomatology instruments, reusable - other
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000030743

Other devices from Lascod S.P.A. (Laboratori Scientifici Odontoiatria)

See all devices from Lascod S.P.A. (Laboratori Scientifici Odontoiatria) →

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