GUDIDData
eudamed_udi Primary ID: 06925794592217

ALANINE AMINOTRANSFERASE LIQUID KIT(IFCC METHOD) (UDI 06925794592217)

Manufactured by DIRUI INDUSTRIAL CO., LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ALANINE AMINOTRANSFERASE LIQUID KIT(IFCC METHOD) - Primary ID 06925794592217

Device Regulatory Overview

The ALANINE AMINOTRANSFERASE LIQUID KIT(IFCC METHOD) (Model/Catalog Number: 3021654) is a medical device manufactured by DIRUI INDUSTRIAL CO., LTD. This product is indexed under FDA Product Code / Category Classification W01010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3021654
Product Code / EMDN
W01010103
Device Name
ALANINE AMINOTRANSFERASE LIQUID KIT(IFCC METHOD)
Database Sync Date
2026-08-09 16:30:32

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 LIQUID KIT(IFCC METHOD)?

The registered manufacturer of record for ALANINE AMINOTRANSFERASE LIQUID KIT(IFCC METHOD) is DIRUI INDUSTRIAL CO., LTD.

What is the Primary UDI-DI identifier for ALANINE AMINOTRANSFERASE LIQUID KIT(IFCC METHOD)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06925794592217.

What classification code is assigned to this device?

This device is registered under product classification code W01010103.

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