gudid Primary ID: 803108

N/A (UDI 803108)

Manufactured by MEDTRONIC SOFAMOR DANEK, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The N/A (Model/Catalog Number: 803108) is a medical device manufactured by MEDTRONIC SOFAMOR DANEK, INC.. This product is indexed under FDA Product Code / Category Classification HAW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 803108
Product Code / EMDN: HAW
Device Name: INSTRUMENT 803-108 GUIDEWIRE INSERTER
Database Sync Date: 2026-08-09 09:08:29

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 N/A?

The registered manufacturer of record for N/A is MEDTRONIC SOFAMOR DANEK, INC..

What is the Primary UDI-DI identifier for N/A?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 803108.

What classification code is assigned to this device?

This device is registered under product classification code HAW.

Similar Classification Devices (HAW)

Other Devices by MEDTRONIC SOFAMOR DANEK, INC.

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