ALKALINE PHOSPHATASE REAGENT KIT（IFCC METHOD） (UDI 06925794592699)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The ALKALINE PHOSPHATASE REAGENT KIT（IFCC METHOD） (Model/Catalog Number: 3021584) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3021584
- Product Code / EMDN
- W01010105
- Device Name
- ALKALINE PHOSPHATASE REAGENT KIT（IFCC METHOD）
- Database Sync Date
- 2026-08-09 16:30:30
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 ALKALINE PHOSPHATASE REAGENT KIT（IFCC METHOD）?
The registered manufacturer of record for ALKALINE PHOSPHATASE REAGENT KIT（IFCC METHOD） is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for ALKALINE PHOSPHATASE REAGENT KIT（IFCC METHOD）?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925794592699.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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