BioCLIA Autoimmune Reagent Kit, RF IgM (UDI 06924030402969)
Manufactured by HOB Biotech Group Corp., Ltd.
Device Regulatory Overview
The BioCLIA Autoimmune Reagent Kit, RF IgM (Model/Catalog Number: MY00181) is a medical device manufactured by HOB Biotech Group Corp., Ltd.. This product is indexed under FDA Product Code / Category Classification W01021110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MY00181
- Product Code / EMDN
- W01021110
- Device Name
- BioCLIA Autoimmune Reagent Kit, RF IgM
- Database Sync Date
- 2026-08-09 16:47:05
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 BioCLIA Autoimmune Reagent Kit, RF IgM?
The registered manufacturer of record for BioCLIA Autoimmune Reagent Kit, RF IgM is HOB Biotech Group Corp., Ltd..
What is the Primary UDI-DI identifier for BioCLIA Autoimmune Reagent Kit, RF IgM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06924030402969.
What classification code is assigned to this device?
This device is registered under product classification code W01021110.
Similar Classification Devices (W01021110)
Other Devices by HOB Biotech Group Corp., Ltd.
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