MAGNESIUM REAGENT KIT（XYLIDYL BLUE METHOD） (UDI 06942202260438)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The MAGNESIUM REAGENT KIT（XYLIDYL BLUE METHOD） (Model/Catalog Number: 3016542) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3016542
- Product Code / EMDN
- W01010299
- Device Name
- MAGNESIUM REAGENT KIT（XYLIDYL BLUE METHOD）
- Database Sync Date
- 2026-08-09 16:29:22
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 MAGNESIUM REAGENT KIT（XYLIDYL BLUE METHOD）?
The registered manufacturer of record for MAGNESIUM REAGENT KIT（XYLIDYL BLUE METHOD） is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for MAGNESIUM REAGENT KIT（XYLIDYL BLUE METHOD）?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202260438.
What classification code is assigned to this device?
This device is registered under product classification code W01010299.
Similar Classification Devices (W01010299)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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