eudamed_udi Primary ID: 05415168001038

Albumin urine & CSF (UDI 05415168001038)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Albumin urine & CSF (Model/Catalog Number: MATUR-L00/AU) is a medical device manufactured by Diagam S.A.. This product is indexed under FDA Product Code / Category Classification W0102010309 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MATUR-L00/AU
Product Code / EMDN: W0102010309
Device Name: Albumin urine & CSF
Database Sync Date: 2026-08-09 16:30:02

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 Albumin urine & CSF?

The registered manufacturer of record for Albumin urine & CSF is Diagam S.A..

What is the Primary UDI-DI identifier for Albumin urine & CSF?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05415168001038.

What classification code is assigned to this device?

This device is registered under product classification code W0102010309.

Similar Classification Devices (W0102010309)

Other Devices by Diagam S.A.

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