eudamed_udi
Primary ID: 04050598007840
ImmuTube® Vitamin D duo (UDI 04050598007840)
Manufactured by Immundiagnostik AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ImmuTube® Vitamin D duo - Primary ID 04050598007840
Device Regulatory Overview
The ImmuTube® Vitamin D duo (Model/Catalog Number: KM1310) 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
- KM1310
- Product Code / EMDN
- W0102060309
- Device Name
- ImmuTube® Vitamin D duo LC-MS/MS kit
- Database Sync Date
- 2026-08-09 16:29:56
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ImmuTube® Vitamin D duo?
The registered manufacturer of record for ImmuTube® Vitamin D duo is Immundiagnostik AG.
What is the Primary UDI-DI identifier for ImmuTube® Vitamin D duo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050598007840.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint