eudamed_udi
Primary ID: 05204309057825
B2 MICROGLOBULIN (UDI 05204309057825)
Manufactured by Medicon Hellas SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for B2 MICROGLOBULIN - Primary ID 05204309057825
Device Regulatory Overview
The B2 MICROGLOBULIN (Model/Catalog Number: 1418-0865) is a medical device manufactured by Medicon Hellas SA. This product is indexed under FDA Product Code / Category Classification W0102039002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1418-0865
- Product Code / EMDN
- W0102039002
- Device Name
- B2 MICROGLOBULIN
- Database Sync Date
- 2026-08-09 17:19:23
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 B2 MICROGLOBULIN?
The registered manufacturer of record for B2 MICROGLOBULIN is Medicon Hellas SA.
What is the Primary UDI-DI identifier for B2 MICROGLOBULIN?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05204309057825.
What classification code is assigned to this device?
This device is registered under product classification code W0102039002.
Similar Classification Devices (W0102039002)
Other Devices by Medicon Hellas SA
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