GUDIDData
eudamed_udi Primary ID: G458292000DN

Alanine aminotransferase (ALT/GPT) - Liquizyme (4+1) (UDI G458292000DN)

Manufactured by Spectrum for Diagnostic Industries (Joint Stock Company)

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Alanine aminotransferase (ALT/GPT) - Liquizyme (4+1) - Primary ID G458292000DN

Device Regulatory Overview

The Alanine aminotransferase (ALT/GPT) - Liquizyme (4+1) (Model/Catalog Number: 292 000) is a medical device manufactured by Spectrum for Diagnostic Industries (Joint Stock Company). This product is indexed under FDA Product Code / Category Classification W01010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
292 000
Product Code / EMDN
W01010103
Device Name
Alanine aminotransferase (ALT/GPT) - Liquizyme (4+1)
Database Sync Date
2026-08-09 16:30:18

Full Regulatory Attributes

🔒 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 Alanine aminotransferase (ALT/GPT) - Liquizyme (4+1)?

The registered manufacturer of record for Alanine aminotransferase (ALT/GPT) - Liquizyme (4+1) is Spectrum for Diagnostic Industries (Joint Stock Company).

What is the Primary UDI-DI identifier for Alanine aminotransferase (ALT/GPT) - Liquizyme (4+1)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G458292000DN.

What classification code is assigned to this device?

This device is registered under product classification code W01010103.

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