GUDIDData
eudamed_udi Primary ID: 08680018942633

Anatolia Geneworks (UDI 08680018942633)

Manufactured by Anatolia Tani ve Biyoteknoloji Urunleri Arastirma Gelistirme San. ve Tic. A.S.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anatolia Geneworks - Primary ID 08680018942633

Device Regulatory Overview

The Anatolia Geneworks (Model/Catalog Number: ABCMQ2) 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 W0105040205 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ABCMQ2
Product Code / EMDN
W0105040205
Device Name
Bosphore CMV Quantification Kit
Database Sync Date
2026-08-09 19:06:45

Full Regulatory Attributes

🔒 Token Gated
{
    "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 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 08680018942633.

What classification code is assigned to this device?

This device is registered under product classification code W0105040205.

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