gudid Primary ID: 01.57.472624

EMG/Stimulation sensor (UDI 01.57.472624)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EMG/Stimulation sensor (Model/Catalog Number: 01.57.472624) is a medical device manufactured by Edan Instruments, Inc.. This product is indexed under FDA Product Code / Category Classification IPF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 01.57.472624
Product Code / EMDN: IPF
Device Name
Database Sync Date: 2026-08-09 09:11:05

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 EMG/Stimulation sensor?

The registered manufacturer of record for EMG/Stimulation sensor is Edan Instruments, Inc..

What is the Primary UDI-DI identifier for EMG/Stimulation sensor?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01.57.472624.

What classification code is assigned to this device?

This device is registered under product classification code IPF.

Similar Classification Devices (IPF)

Other Devices by Edan Instruments, Inc.

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