GLYCOHEMOGLOBIN A 1C REAGENT KIT (UDI 06942202261626)
Manufactured by DIRUI INDUSTRIAL CO., LTD
Device Regulatory Overview
The GLYCOHEMOGLOBIN A 1C REAGENT KIT (Model/Catalog Number: 232021202009) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010214 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 232021202009
- Product Code / EMDN
- W01010214
- Device Name
- GLYCOHEMOGLOBIN A 1C REAGENT KIT
- Database Sync Date
- 2026-08-09 16:29:08
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 GLYCOHEMOGLOBIN A 1C REAGENT KIT?
The registered manufacturer of record for GLYCOHEMOGLOBIN A 1C REAGENT KIT is DIRUI INDUSTRIAL CO., LTD.
What is the Primary UDI-DI identifier for GLYCOHEMOGLOBIN A 1C REAGENT KIT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942202261626.
What classification code is assigned to this device?
This device is registered under product classification code W01010214.
Similar Classification Devices (W01010214)
Other Devices by DIRUI INDUSTRIAL CO., LTD
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