eudamed_udi Primary ID: 62230041002842

Alkaline Phosphatase (ALP) -Colorimetric (UDI 62230041002842)

Manufactured by Egyptian Company For Biotechnology-Spectrum Diagnostics

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Alkaline Phosphatase (ALP) -Colorimetric (Model/Catalog Number: 216 001) is a medical device manufactured by Egyptian Company For Biotechnology-Spectrum Diagnostics. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 216 001
Product Code / EMDN: W01010105
Device Name: Alkaline Phosphatase (ALP) -Colorimetric
Database Sync Date: 2026-08-09 16:58:12

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Alkaline Phosphatase (ALP) -Colorimetric?

The registered manufacturer of record for Alkaline Phosphatase (ALP) -Colorimetric is Egyptian Company For Biotechnology-Spectrum Diagnostics.

What is the Primary UDI-DI identifier for Alkaline Phosphatase (ALP) -Colorimetric?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 62230041002842.

What classification code is assigned to this device?

This device is registered under product classification code W01010105.

Similar Classification Devices (W01010105)

Other Devices by Egyptian Company For Biotechnology-Spectrum Diagnostics

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint