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Atlas

by Atlas Cerrahi̇ Aletler Ltd. Şti̇. Türkiye EUDAMED

Ref F15 83-36Model ATLAS

EMDN L091302

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868377950ATLAS386F Basic UDI-DIDate9 Jan 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Reverser
Model / Reference
ATLAS, F15 83-36
Primary DI / UDI-DI
08683255354047
Basic UDI-DI
868377950ATLAS386F
EMDN Code
L091302 Bone rongeurs, reusable
Device Class
Class I
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020246

Other devices from Atlas Cerrahi̇ Aletler Ltd. Şti̇.

See all devices from Atlas Cerrahi̇ Aletler Ltd. Şti̇. →

Properties & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED 628995c9-5163-44e8-abbe-b5e67eef0af4 61 fields · synced 24 Oct 2026