gudid Primary ID: 07-APD-1020

MATIRA ANTERIOR CERVICAL SYSTEM (UDI 07-APD-1020)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MATIRA ANTERIOR CERVICAL SYSTEM (Model/Catalog Number: 07-APD-1020) is a medical device manufactured by Kalitec Direct LLC. This product is indexed under FDA Product Code / Category Classification GCZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 07-APD-1020
Product Code / EMDN: GCZ
Device Name: Temporary Pin, BMA Disposable
Database Sync Date: 2026-08-09 09:51:04

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 MATIRA ANTERIOR CERVICAL SYSTEM?

The registered manufacturer of record for MATIRA ANTERIOR CERVICAL SYSTEM is Kalitec Direct LLC.

What is the Primary UDI-DI identifier for MATIRA ANTERIOR CERVICAL SYSTEM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07-APD-1020.

What classification code is assigned to this device?

This device is registered under product classification code GCZ.

Similar Classification Devices (GCZ)

Other Devices by Kalitec Direct LLC

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