NA (UDI 446.918)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: 446.918) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification GXR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 446.918
Product Code / EMDN: GXR
Device Name: 1.5MM TI CHIN PLATE-DOUBLE BEND 6 HOLES/6MM ADVANCEMENT
Database Sync Date: 2026-08-09 09:39:06

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 NA?

The registered manufacturer of record for NA is Synthes GmbH.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 446.918.

What classification code is assigned to this device?

This device is registered under product classification code GXR.

Similar Classification Devices (GXR)

Other Devices by Synthes GmbH

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