GUDIDData
eudamed_udi Primary ID: 84352873053174

Cromatest (UDI 84352873053174)

Manufactured by Linear Chemicals S.L.U

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cromatest - Primary ID 84352873053174

Device Regulatory Overview

The Cromatest (Model/Catalog Number: 1953005) is a medical device manufactured by Linear Chemicals S.L.U. This product is indexed under FDA Product Code / Category Classification W0101050303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1953005
Product Code / EMDN
W0101050303
Device Name
Total Protein Standard
Database Sync Date
2026-08-09 16:59:44

Full Regulatory Attributes

๐Ÿ”’ Token Gated
{
    "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 Cromatest?

The registered manufacturer of record for Cromatest is Linear Chemicals S.L.U.

What is the Primary UDI-DI identifier for Cromatest?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 84352873053174.

What classification code is assigned to this device?

This device is registered under product classification code W0101050303.

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