GLUCOSE REAGENT KIT(GLUCOSE OXIDASE METHOD) (UDI 06942202259944)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The GLUCOSE REAGENT KIT(GLUCOSE OXIDASE METHOD) (Model/Catalog Number: 3021158) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010213 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3021158
- Product Code / EMDN
- W01010213
- Device Name
- GLUCOSE REAGENT KIT(GLUCOSE OXIDASE METHOD)
- Database Sync Date
- 2026-08-09 16:29:18
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 GLUCOSE REAGENT KIT(GLUCOSE OXIDASE METHOD)?
The registered manufacturer of record for GLUCOSE REAGENT KIT(GLUCOSE OXIDASE METHOD) is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for GLUCOSE REAGENT KIT(GLUCOSE OXIDASE METHOD)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202259944.
What classification code is assigned to this device?
This device is registered under product classification code W01010213.
Similar Classification Devices (W01010213)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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