β2-Microprotein (BMG) Test Kit (Latex Immunoturbidimetric) (UDI 06936895308041)
Manufactured by Biobase Biodustry(Shandong) Co.,Ltd.
Device Regulatory Overview
The β2-Microprotein (BMG) Test Kit (Latex Immunoturbidimetric) (Model/Catalog Number: R1:48mL×2 R2:32mL×1（793）) is a medical device manufactured by Biobase Biodustry(Shandong) 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
- R1:48mL×2 R2:32mL×1（793）
- Product Code / EMDN
- W0102039002
- Device Name
- β2-Microprotein (BMG) Test Kit (Latex Immunoturbidimetric)
- Database Sync Date
- 2026-08-09 17:41:41
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-Microprotein (BMG) Test Kit (Latex Immunoturbidimetric)?
The registered manufacturer of record for β2-Microprotein (BMG) Test Kit (Latex Immunoturbidimetric) is Biobase Biodustry(Shandong) Co.,Ltd..
What is the Primary UDI-DI identifier for β2-Microprotein (BMG) Test Kit (Latex Immunoturbidimetric)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936895308041.
What classification code is assigned to this device?
This device is registered under product classification code W0102039002.
Similar Classification Devices (W0102039002)
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