eudamed_udi Primary ID: 05415168005920

Alpha2-macroglobulin (UDI 05415168005920)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Alpha2-macroglobulin (Model/Catalog Number: MGTUR-L00/ATE) is a medical device manufactured by Diagam S.A.. This product is indexed under FDA Product Code / Category Classification W0102019003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MGTUR-L00/ATE
Product Code / EMDN: W0102019003
Device Name: Alpha2-macroglobulin
Database Sync Date: 2026-08-09 16:28:59

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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Frequently Asked Questions

Who is the primary manufacturer of Alpha2-macroglobulin?

The registered manufacturer of record for Alpha2-macroglobulin is Diagam S.A..

What is the Primary UDI-DI identifier for Alpha2-macroglobulin?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415168005920.

What classification code is assigned to this device?

This device is registered under product classification code W0102019003.

Similar Classification Devices (W0102019003)

Other Devices by Diagam S.A.

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