EUROLINE-WB Anti-Echinococcus (IgG) (UDI DY 2321-4801-2 G)
Manufactured by EUROIMMUN Medizinische Labordiagnostika AG
Device Regulatory Overview
The EUROLINE-WB Anti-Echinococcus (IgG) (Model/Catalog Number: DY 2321-4801-2 G) is a medical device manufactured by EUROIMMUN Medizinische Labordiagnostika AG. This product is indexed under FDA Product Code / Category Classification GPE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DY 2321-4801-2 G
- Product Code / EMDN
- GPE
- Device Name
- Database Sync Date
- 2026-08-09 09:11:29
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 EUROLINE-WB Anti-Echinococcus (IgG)?
The registered manufacturer of record for EUROLINE-WB Anti-Echinococcus (IgG) is EUROIMMUN Medizinische Labordiagnostika AG.
What is the Primary UDI-DI identifier for EUROLINE-WB Anti-Echinococcus (IgG)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DY 2321-4801-2 G.
What classification code is assigned to this device?
This device is registered under product classification code GPE.
Similar Classification Devices (GPE)
Other Devices by EUROIMMUN Medizinische Labordiagnostika AG
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