eudamed_udi Primary ID: 8053617720122ZF

Alkaline Phosphatase DGKC LS (UDI 8053617720122ZF)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Alkaline Phosphatase DGKC LS (Model/Catalog Number: CC1015 - CC1016 - CC1017) is a medical device manufactured by MTD Diagnostics srl. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CC1015 - CC1016 - CC1017
Product Code / EMDN: W01010105
Device Name: Alkaline Phosphatase DGKC LS
Database Sync Date: 2026-08-09 16:59:00

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 Alkaline Phosphatase DGKC LS?

The registered manufacturer of record for Alkaline Phosphatase DGKC LS is MTD Diagnostics srl.

What is the Primary UDI-DI identifier for Alkaline Phosphatase DGKC LS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8053617720122ZF.

What classification code is assigned to this device?

This device is registered under product classification code W01010105.

Similar Classification Devices (W01010105)

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