gudid Primary ID: 10-4032-10NKM

DENVER SPLINT (UDI 10-4032-10NKM)

Manufactured by SHIPPERT MEDICAL TECHNOLOGIES, INC

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DENVER SPLINT (Model/Catalog Number: 10-4032-10NKM) is a medical device manufactured by SHIPPERT MEDICAL TECHNOLOGIES, INC. This product is indexed under FDA Product Code / Category Classification EPP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10-4032-10NKM
Product Code / EMDN: EPP
Device Name
Database Sync Date: 2026-08-09 09:22:09

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 DENVER SPLINT?

The registered manufacturer of record for DENVER SPLINT is SHIPPERT MEDICAL TECHNOLOGIES, INC.

What is the Primary UDI-DI identifier for DENVER SPLINT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-4032-10NKM.

What classification code is assigned to this device?

This device is registered under product classification code EPP.

Similar Classification Devices (EPP)

Other Devices by SHIPPERT MEDICAL TECHNOLOGIES, INC

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