eudamed_udi
Primary ID: 04050598008830
IDK® 25-OH-Vitamin D ELISA (UDI 04050598008830)
Manufactured by Immundiagnostik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IDK® 25-OH-Vitamin D ELISA - Primary ID 04050598008830
Device Regulatory Overview
The IDK® 25-OH-Vitamin D ELISA (Model/Catalog Number: K 2020DBS) is a medical device manufactured by Immundiagnostik AG. This product is indexed under FDA Product Code / Category Classification W0102060309 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K 2020DBS
- Product Code / EMDN
- W0102060309
- Device Name
- IDK® 25-OH-Vitamin D ELISA
- Database Sync Date
- 2026-08-09 16:47:20
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® 25-OH-Vitamin D ELISA?
The registered manufacturer of record for IDK® 25-OH-Vitamin D ELISA is Immundiagnostik AG.
What is the Primary UDI-DI identifier for IDK® 25-OH-Vitamin D ELISA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050598008830.
What classification code is assigned to this device?
This device is registered under product classification code W0102060309.
Similar Classification Devices (W0102060309)
Other Devices by Immundiagnostik AG
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