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Atlas

by Atlas Cerrahi̇ Aletler Ltd. Şti̇. 1,000+ variants

Ref B22 12-42Model ATLAS

Atlas (B22 12-42) is a Class I device made by Atlas Cerrahi̇ Aletler Ltd. Şti̇., registered in EUDAMED on 9 Jan 2024 (Basic UDI-DI 868377950ATLAS9973), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

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

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number868377950ATLAS9973 Basic UDI-DI 08683255330669UDI-DIDate9 Jan 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Seperator
Model / reference
ATLAS, B22 12-42
Primary DI / UDI-DI
08683255330669
Basic UDI-DI
868377950ATLAS9973
EMDN code
L03140199 Spreaders and retractors for general surgery, reusable - other
Device class
Class I
EU registration type
Standard device
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000020246

Related devices

Category: Hand-held surgical retractor, reusable

Similar devices in this category

Other devices filed under SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER.

Other devices from Atlas Cerrahi̇ Aletler Ltd. Şti̇.

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

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)