eudamed_udi
Primary ID: 08683255354306
ATLAS (UDI 08683255354306)
Manufactured by ATLAS CERRAHİ ALETLER LTD. ŞTİ.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ATLAS - Primary ID 08683255354306
Device Regulatory Overview
The ATLAS (Model/Catalog Number: F15 93-70) is a medical device manufactured by ATLAS CERRAHİ ALETLER LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification L091302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- F15 93-70
- Product Code / EMDN
- L091302
- Device Name
- REVERSER
- Database Sync Date
- 2026-08-09 16:29:16
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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Get API Token Access ($49/mo)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 08683255354306.
What classification code is assigned to this device?
This device is registered under product classification code L091302.
Similar Classification Devices (L091302)
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