Electrical Stimulator AUDIOTRON (UDI 04571292660938)
Manufactured by OG Wellness Technologies Co., Ltd. Headquarters
Device Regulatory Overview
The Electrical Stimulator AUDIOTRON (Model/Catalog Number: －) is a medical device manufactured by OG Wellness Technologies Co., Ltd. Headquarters. This product is indexed under FDA Product Code / Category Classification Z120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- －
- Product Code / EMDN
- Z120601
- Device Name
- Electrical Stimulator AUDIOTRON
- Database Sync Date
- 2026-08-09 17:03:46
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Electrical Stimulator AUDIOTRON?
The registered manufacturer of record for Electrical Stimulator AUDIOTRON is OG Wellness Technologies Co., Ltd. Headquarters.
What is the Primary UDI-DI identifier for Electrical Stimulator AUDIOTRON?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04571292660938.
What classification code is assigned to this device?
This device is registered under product classification code Z120601.
Similar Classification Devices (Z120601)
Other Devices by OG Wellness Technologies Co., Ltd. Headquarters
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint