eudamed_udi
Primary ID: 08683255339389
ATLAS (UDI 08683255339389)
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 08683255339389
Device Regulatory Overview
The ATLAS (Model/Catalog Number: E13 39-03) is a medical device manufactured by ATLAS CERRAHİ ALETLER LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification L060412 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- E13 39-03
- Product Code / EMDN
- L060412
- Device Name
- SEPERATOR
- Database Sync Date
- 2026-08-09 16:50:38
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 08683255339389.
What classification code is assigned to this device?
This device is registered under product classification code L060412.
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