gudid Primary ID: NS-6000-4002

Contracture Management (UDI NS-6000-4002)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Contracture Management (Model/Catalog Number: NS-6000-4002) is a medical device manufactured by ORTHOPEDIATRICS CORP.. This product is indexed under FDA Product Code / Category Classification IQI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NS-6000-4002
Product Code / EMDN: IQI
Device Name: Hinge Assembly Pediatric, Right
Database Sync Date: 2026-08-09 09:14:02

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 Contracture Management?

The registered manufacturer of record for Contracture Management is ORTHOPEDIATRICS CORP..

What is the Primary UDI-DI identifier for Contracture Management?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NS-6000-4002.

What classification code is assigned to this device?

This device is registered under product classification code IQI.

Similar Classification Devices (IQI)

Other Devices by ORTHOPEDIATRICS CORP.

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