GUDIDData
eudamed_udi Primary ID: 08683555612434

Anti-Streptolysin O [ASO] (UDI 08683555612434)

Manufactured by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anti-Streptolysin O [ASO] - Primary ID 08683555612434

Device Regulatory Overview

The Anti-Streptolysin O [ASO] (Model/Catalog Number: B27033) is a medical device manufactured by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification W02029099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
B27033
Product Code / EMDN
W02029099
Device Name
Anti-Streptolysin O [ASO] Kit
Database Sync Date
2026-08-09 17:30:12

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 Anti-Streptolysin O [ASO]?

The registered manufacturer of record for Anti-Streptolysin O [ASO] is KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for Anti-Streptolysin O [ASO]?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683555612434.

What classification code is assigned to this device?

This device is registered under product classification code W02029099.

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