gudid Primary ID: MI-001F

N/A (UDI MI-001F)

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: MI-001F) is a medical device manufactured by MEDTRONIC SOFAMOR DANEK, INC.. This product is indexed under FDA Product Code / Category Classification MAX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MI-001F
Product Code / EMDN: MAX
Device Name: LOOP INSERTER TUBE
Database Sync Date: 2026-08-09 09:11:39

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 MI-001F.

What classification code is assigned to this device?

This device is registered under product classification code MAX.

Similar Classification Devices (MAX)

Other Devices by MEDTRONIC SOFAMOR DANEK, INC.

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