eudamed_udi
Primary ID: 05204309104772
FERRITIN CALIBRATOR (UDI 05204309104772)
Manufactured by Medicon Hellas SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FERRITIN CALIBRATOR - Primary ID 05204309104772
Device Regulatory Overview
The FERRITIN CALIBRATOR (Model/Catalog Number: 1478-0275) is a medical device manufactured by Medicon Hellas SA. This product is indexed under FDA Product Code / Category Classification W0102152206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1478-0275
- Product Code / EMDN
- W0102152206
- Device Name
- FERRITIN
- Database Sync Date
- 2026-08-09 16:58:24
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 FERRITIN CALIBRATOR?
The registered manufacturer of record for FERRITIN CALIBRATOR is Medicon Hellas SA.
What is the Primary UDI-DI identifier for FERRITIN CALIBRATOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204309104772.
What classification code is assigned to this device?
This device is registered under product classification code W0102152206.
Similar Classification Devices (W0102152206)
Other Devices by Medicon Hellas SA
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