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Wkręty Kaniulowane Podskokowe

by ChM spółka z ograniczoną odpowiedzialnością 32 variants

Ref 3.1731.000SModel CANNULATED SUBTALAR SCREWS

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59084474NSP7.7T2 Basic UDI-DI 05908447347588UDI-DIDate14 Jul 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  • Withdrawn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
Wkręty Kaniulowane Podskokowe
Model / Reference
CANNULATED SUBTALAR SCREWS, 3.1731.000S
Primary DI / UDI-DI
05908447347588
Basic UDI-DI
59084474NSP7.7T2
Direct Marketing DI
05908447347588
EMDN Code
P09120699 Bone fixation screws, tendon and ligament synthesis screws - other
Device Class
Class IIb
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000002121

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Properties

  • Sterile
  • Implantable
  • Sutures

Other properties (11)

  • 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