gudid Primary ID: CURIX ORTHO REGULAR 24X30

CURIX ORTHO REGULAR (UDI CURIX ORTHO REGULAR 24X30)

Manufactured by AGFA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CURIX ORTHO REGULAR (Model/Catalog Number: CURIX ORTHO REGULAR 24X30) is a medical device manufactured by AGFA. This product is indexed under FDA Product Code / Category Classification IXA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CURIX ORTHO REGULAR 24X30
Product Code / EMDN: IXA
Device Name: CURIX CAS US+OR REG 24X30
Database Sync Date: 2026-08-09 09:57:24

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 CURIX ORTHO REGULAR?

The registered manufacturer of record for CURIX ORTHO REGULAR is AGFA.

What is the Primary UDI-DI identifier for CURIX ORTHO REGULAR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CURIX ORTHO REGULAR 24X30.

What classification code is assigned to this device?

This device is registered under product classification code IXA.

Similar Classification Devices (IXA)

Other Devices by AGFA

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