eudamed_udi Primary ID: 62230182707514

Alkaline Phosphatase (Single Reagent) (Kinetic IFCC Method) (UDI 62230182707514)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Alkaline Phosphatase (Single Reagent) (Kinetic IFCC Method) (Model/Catalog Number: D-603 004) is a medical device manufactured by Kalians Corporation. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: D-603 004
Product Code / EMDN: W01010105
Device Name: Alkaline Phosphatase (Single Reagent) (Kinetic IFCC Method)
Database Sync Date: 2026-08-09 17:06:40

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 (Single Reagent) (Kinetic IFCC Method)?

The registered manufacturer of record for Alkaline Phosphatase (Single Reagent) (Kinetic IFCC Method) is Kalians Corporation.

What is the Primary UDI-DI identifier for Alkaline Phosphatase (Single Reagent) (Kinetic IFCC Method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 62230182707514.

What classification code is assigned to this device?

This device is registered under product classification code W01010105.

Similar Classification Devices (W01010105)

Other Devices by Kalians Corporation

Programmatic Export

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

JSON API Endpoint