eudamed_udi Primary ID: D-C0159LS

Albumin (UDI D-C0159LS)

Manufactured by C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Albumin (Model/Catalog Number: C0159) is a medical device manufactured by C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.. This product is indexed under FDA Product Code / Category Classification W01010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: C0159
Product Code / EMDN: W01010201
Device Name: Albumin
Database Sync Date: 2026-08-09 16:48:57

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?

The registered manufacturer of record for Albumin is C.P.M. COMPAGNIA PER LA MEDICINA S.R.L..

What is the Primary UDI-DI identifier for Albumin?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-C0159LS.

What classification code is assigned to this device?

This device is registered under product classification code W01010201.

Similar Classification Devices (W01010201)

Other Devices by C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.

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