eudamed_udi Primary ID: 00866489000067

Procleix Reagent Preparation Incubator 250 (UDI 00866489000067)

Manufactured by Grifols Diagnostic Solutions Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Procleix Reagent Preparation Incubator 250 (Model/Catalog Number: 740820) is a medical device manufactured by Grifols Diagnostic Solutions Inc.. This product is indexed under FDA Product Code / Category Classification W02079099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 740820
Product Code / EMDN: W02079099
Device Name: Procleix Reagent Preparation Incubator 250
Database Sync Date: 2026-08-09 17:08:01

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 Procleix Reagent Preparation Incubator 250?

The registered manufacturer of record for Procleix Reagent Preparation Incubator 250 is Grifols Diagnostic Solutions Inc..

What is the Primary UDI-DI identifier for Procleix Reagent Preparation Incubator 250?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00866489000067.

What classification code is assigned to this device?

This device is registered under product classification code W02079099.

Similar Classification Devices (W02079099)

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