Anatolia Geneworks (UDI 08680018946334)
Manufactured by Anatolia Tani ve Biyoteknoloji Urunleri Arastirma Gelistirme San. ve Tic. A.S.
Device Regulatory Overview
The Anatolia Geneworks (Model/Catalog Number: AE96WG) is a medical device manufactured by Anatolia Tani ve Biyoteknoloji Urunleri Arastirma Gelistirme San. ve Tic. A.S.. This product is indexed under FDA Product Code / Category Classification W0105900101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AE96WG
- Product Code / EMDN
- W0105900101
- Device Name
- Magnesia 2448 Whole Blood Genomic DNA Extraction Kit
- Database Sync Date
- 2026-08-09 16:29:00
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 Anatolia Geneworks?
The registered manufacturer of record for Anatolia Geneworks is Anatolia Tani ve Biyoteknoloji Urunleri Arastirma Gelistirme San. ve Tic. A.S..
What is the Primary UDI-DI identifier for Anatolia Geneworks?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680018946334.
What classification code is assigned to this device?
This device is registered under product classification code W0105900101.
Similar Classification Devices (W0105900101)
Other Devices by Anatolia Tani ve Biyoteknoloji Urunleri Arastirma Gelistirme San. ve Tic. A.S.
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