eudamed_udi Primary ID: 08683255381906

ATLAS (UDI 08683255381906)

Manufactured by ATLAS CERRAHİ ALETLER LTD. ŞTİ.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ATLAS (Model/Catalog Number: B03 56-16P) is a medical device manufactured by ATLAS CERRAHİ ALETLER LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification L010499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: B03 56-16P
Product Code / EMDN: L010499
Device Name: CUTTER
Database Sync Date: 2026-08-09 16:29:05

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of ATLAS?

The registered manufacturer of record for ATLAS is ATLAS CERRAHİ ALETLER LTD. ŞTİ..

What is the Primary UDI-DI identifier for ATLAS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683255381906.

What classification code is assigned to this device?

This device is registered under product classification code L010499.

Similar Classification Devices (L010499)

Other Devices by ATLAS CERRAHİ ALETLER LTD. ŞTİ.

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