gudid Primary ID: 54-225

Cross-Hair Reticule, XRETIC (UDI 54-225)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Cross-Hair Reticule, XRETIC (Model/Catalog Number: 54-225) is a medical device manufactured by Aktina Corp.. This product is indexed under FDA Product Code / Category Classification IWE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 54-225
Product Code / EMDN: IWE
Device Name
Database Sync Date: 2026-08-09 09:18:01

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 Cross-Hair Reticule, XRETIC?

The registered manufacturer of record for Cross-Hair Reticule, XRETIC is Aktina Corp..

What is the Primary UDI-DI identifier for Cross-Hair Reticule, XRETIC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 54-225.

What classification code is assigned to this device?

This device is registered under product classification code IWE.

Similar Classification Devices (IWE)

Other Devices by Aktina Corp.

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