DIRECT BILIRUBIN REAGENT KIT(DIAZO SALT METHOD) (UDI 06942202259081)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The DIRECT BILIRUBIN REAGENT KIT(DIAZO SALT METHOD) (Model/Catalog Number: 3016507) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3016507
- Product Code / EMDN
- W01010203
- Device Name
- DIRECT BILIRUBIN REAGENT KIT(DIAZO SALT METHOD)
- Database Sync Date
- 2026-08-09 16:30:14
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 DIRECT BILIRUBIN REAGENT KIT(DIAZO SALT METHOD)?
The registered manufacturer of record for DIRECT BILIRUBIN REAGENT KIT(DIAZO SALT METHOD) is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for DIRECT BILIRUBIN REAGENT KIT(DIAZO SALT METHOD)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202259081.
What classification code is assigned to this device?
This device is registered under product classification code W01010203.
Similar Classification Devices (W01010203)
Other Devices by DIRUI INDUSTRIAL CO., LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint