GUDIDData
eudamed_udi Primary ID: 05060481691468

SX230FW EMG Sensor (Gain 1000, Bandwidth 20-460Hz) - Plastic connector (UDI 05060481691468)

Manufactured by Biometrics Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SX230FW EMG Sensor (Gain 1000, Bandwidth 20-460Hz) - Plastic connector - Primary ID 05060481691468

Device Regulatory Overview

The SX230FW EMG Sensor (Gain 1000, Bandwidth 20-460Hz) - Plastic connector (Model/Catalog Number: SX230FW) is a medical device manufactured by Biometrics Ltd. This product is indexed under FDA Product Code / Category Classification N010101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SX230FW
Product Code / EMDN
N010101
Device Name
Data Acquisition Products
Database Sync Date
2026-08-09 17:35:07

Full Regulatory Attributes

🔒 Token Gated
{
    "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 SX230FW EMG Sensor (Gain 1000, Bandwidth 20-460Hz) - Plastic connector?

The registered manufacturer of record for SX230FW EMG Sensor (Gain 1000, Bandwidth 20-460Hz) - Plastic connector is Biometrics Ltd.

What is the Primary UDI-DI identifier for SX230FW EMG Sensor (Gain 1000, Bandwidth 20-460Hz) - Plastic connector?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060481691468.

What classification code is assigned to this device?

This device is registered under product classification code N010101.

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