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FFX ancillary

by Sc Medica 19 variants

Ref 58.EXX.XXM

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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number377001950357001DE Basic UDI-DI Date20 Apr 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
FFX ancillary
Model / Reference
58.EXX.XXM
Primary DI / UDI-DI
03770019503805, 03770019503713, 03770019503959, 03770019503690, 03760418040452, 03770019503966, 03770019503706, 03770019503829
Basic UDI-DI
377001950357001DE
Direct Marketing DI
03770019503805
03770019503713
03770019503959
03770019503690
03760418040452
03770019503966
03770019503706
03770019503829
EMDN Code
L26 Surgical screwdrivers, reusable
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000002722

Other devices from Sc Medica

See all devices from Sc Medica →

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