GUDIDData
gudid Primary ID: 714.08.83

MediRod Pedicle Screw System (UDI 714.08.83)

Manufactured by Medicon eG. Chirurgiemechaniker-Genossenschaft

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MediRod Pedicle Screw System - Primary ID 714.08.83

Device Regulatory Overview

The MediRod Pedicle Screw System (Model/Catalog Number: 714.08.83) is a medical device manufactured by Medicon eG. Chirurgiemechaniker-Genossenschaft. This product is indexed under FDA Product Code / Category Classification NKB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
714.08.83
Product Code / EMDN
NKB
Device Name
mediRod ti iliacale screw 8x100mm
Database Sync Date
2026-08-09 09:43:19

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of MediRod Pedicle Screw System?

The registered manufacturer of record for MediRod Pedicle Screw System is Medicon eG. Chirurgiemechaniker-Genossenschaft.

What is the Primary UDI-DI identifier for MediRod Pedicle Screw System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 714.08.83.

What classification code is assigned to this device?

This device is registered under product classification code NKB.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint