GUDIDData
gudid Primary ID: Ultima 3T+

Ultima 3T+ (UDI Ultima 3T+)

Manufactured by EasyMed Instruments Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ultima 3T+ - Primary ID Ultima 3T+

Device Regulatory Overview

The Ultima 3T+ (Model/Catalog Number: Ultima 3T+) is a medical device manufactured by EasyMed Instruments Co., Ltd.. This product is indexed under FDA Product Code / Category Classification GZJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Ultima 3T+
Product Code / EMDN
GZJ
Device Name
Ultima 3T+ is a Transcutaneous Electrical Nerve Stimulator, which is used to provide symptomatic pain relief for chronic, acute or post operative pain.
Database Sync Date
2026-08-09 09:11:07

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 Ultima 3T+?

The registered manufacturer of record for Ultima 3T+ is EasyMed Instruments Co., Ltd..

What is the Primary UDI-DI identifier for Ultima 3T+?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Ultima 3T+.

What classification code is assigned to this device?

This device is registered under product classification code GZJ.

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