Atlas

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

Ref F11 34-10Model ATLAS

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 24 Oct 2026. What this means

Overview

The ATLAS device is a Class I medical device designed for the separation of tissues, making it an essential tool in various clinical settings. It has undergone thorough professional testing and meets regulatory standards to ensure its safety and efficacy.

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number868377950ATLAS9973 Basic UDI-DI 08683255346318UDI-DI	Date9 Jan 2024Registered	StatusActive

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

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Seperator
Model / Reference: ATLAS, F11 34-10

Primary DI / UDI-DI: 08683255346318
Basic UDI-DI: 868377950ATLAS9973
EMDN Code: L091201 Orthopaedic surgery rasps, reusable

Device Class: Class I
EU market of registration: Türkiye

Manufacturer details

EUDAMED SRN: TR-MF-000020246

Other devices from Atlas Cerrahi̇ Aletler Ltd. Şti̇.

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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