Laminin（LN）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay） (UDI 06974969982285)
Manufactured by Biobase Diagnostic Technology (Shandong) Co., Ltd.
Device Regulatory Overview
The Laminin（LN）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay） (Model/Catalog Number: 200 Tests/kit（DR1074-3）) is a medical device manufactured by Biobase Diagnostic Technology (Shandong) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102039006 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 200 Tests/kit（DR1074-3）
- Product Code / EMDN
- W0102039006
- Device Name
- Laminin（LN）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）
- Database Sync Date
- 2026-08-09 17:07:33
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 Laminin（LN）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）?
The registered manufacturer of record for Laminin（LN）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay） is Biobase Diagnostic Technology (Shandong) Co., Ltd..
What is the Primary UDI-DI identifier for Laminin（LN）Detection Kit（Magnetic Solid Phase Chemiluminescent Immunoassay）?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06974969982285.
What classification code is assigned to this device?
This device is registered under product classification code W0102039006.
Similar Classification Devices (W0102039006)
Other Devices by Biobase Diagnostic Technology (Shandong) Co., Ltd.
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