β2-Microglobulin Reagent Kit (UDI D-B2-MG601SS)
Manufactured by Hangzhou Aichek Medical Technology Co., Ltd.
Device Regulatory Overview
The β2-Microglobulin Reagent Kit (Model/Catalog Number: β2-MG6011Y, β2-MG6012Y, β2-MG6013Y, β2-MG6014Y, β2-MG6015Y, β2-MG6011N, β2-MG6012N, β2-MG6013N, β2-MG6014N, β2-MG6015N) is a medical device manufactured by Hangzhou Aichek Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102039002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- β2-MG6011Y, β2-MG6012Y, β2-MG6013Y, β2-MG6014Y, β2-MG6015Y, β2-MG6011N, β2-MG6012N, β2-MG6013N, β2-MG6014N, β2-MG6015N
- Product Code / EMDN
- W0102039002
- Device Name
- β2-Microglobulin Reagent Kit
- Database Sync Date
- 2026-08-09 17:36:01
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 β2-Microglobulin Reagent Kit?
The registered manufacturer of record for β2-Microglobulin Reagent Kit is Hangzhou Aichek Medical Technology Co., Ltd..
What is the Primary UDI-DI identifier for β2-Microglobulin Reagent Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-B2-MG601SS.
What classification code is assigned to this device?
This device is registered under product classification code W0102039002.
Similar Classification Devices (W0102039002)
Other Devices by Hangzhou Aichek Medical Technology Co., Ltd.
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