CREATININE J Kit (UDI 08683555601889)
Manufactured by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ
Device Regulatory Overview
The CREATININE J Kit (Model/Catalog Number: B28128) is a medical device manufactured by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification W01010207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- B28128
- Product Code / EMDN
- W01010207
- Device Name
- CREATININE J Kit
- Database Sync Date
- 2026-08-09 16:30:10
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of CREATININE J Kit?
The registered manufacturer of record for CREATININE J Kit is KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for CREATININE J Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08683555601889.
What classification code is assigned to this device?
This device is registered under product classification code W01010207.
Similar Classification Devices (W01010207)
Other Devices by KİNETİK BİLİŞİM DİAGNOSTİK ANONİM ŞİRKETİ
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint