eudamed_udi Primary ID: G4582140017U

Alkaline phosphatase (ALP)-Liquizyme (9+1) (UDI G4582140017U)

Manufactured by Spectrum for Diagnostic Industries (Joint Stock Company)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Alkaline phosphatase (ALP)-Liquizyme (9+1) (Model/Catalog Number: 214 001) is a medical device manufactured by Spectrum for Diagnostic Industries (Joint Stock Company). This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 214 001
Product Code / EMDN: W01010105
Device Name: Alkaline phosphatase (ALP)-Liquizyme (9+1)
Database Sync Date: 2026-08-09 16:59:05

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 (ALP)-Liquizyme (9+1)?

The registered manufacturer of record for Alkaline phosphatase (ALP)-Liquizyme (9+1) is Spectrum for Diagnostic Industries (Joint Stock Company).

What is the Primary UDI-DI identifier for Alkaline phosphatase (ALP)-Liquizyme (9+1)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G4582140017U.

What classification code is assigned to this device?

This device is registered under product classification code W01010105.

Similar Classification Devices (W01010105)

Other Devices by Spectrum for Diagnostic Industries (Joint Stock Company)

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