gudid
Primary ID: K 8870.20.US
IDK sIgA ELISA (UDI K 8870.20.US)
Manufactured by Immundiagnostik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IDK sIgA ELISA - Primary ID K 8870.20.US
Device Regulatory Overview
The IDK sIgA ELISA (Model/Catalog Number: K 8870.20.US) is a medical device manufactured by Immundiagnostik AG. This product is indexed under FDA Product Code / Category Classification DAJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K 8870.20.US
- Product Code / EMDN
- DAJ
- Device Name
- Database Sync Date
- 2026-08-09 09:11:21
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 IDK sIgA ELISA?
The registered manufacturer of record for IDK sIgA ELISA is Immundiagnostik AG.
What is the Primary UDI-DI identifier for IDK sIgA ELISA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is K 8870.20.US.
What classification code is assigned to this device?
This device is registered under product classification code DAJ.
Similar Classification Devices (DAJ)
Other Devices by Immundiagnostik AG
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