eudamed_udi
Primary ID: 06947832500749
TENS/EMS Unit (UDI 06947832500749)
Manufactured by Shenzhen Aeon Technology Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TENS/EMS Unit - Primary ID 06947832500749
Device Regulatory Overview
The TENS/EMS Unit (Model/Catalog Number: A621) is a medical device manufactured by Shenzhen Aeon Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12062801 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A621
- Product Code / EMDN
- Z12062801
- Device Name
- TENS/EMS Unit
- Database Sync Date
- 2026-08-09 17:06:52
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of TENS/EMS Unit?
The registered manufacturer of record for TENS/EMS Unit is Shenzhen Aeon Technology Co., Ltd..
What is the Primary UDI-DI identifier for TENS/EMS Unit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06947832500749.
What classification code is assigned to this device?
This device is registered under product classification code Z12062801.
Similar Classification Devices (Z12062801)
Other Devices by Shenzhen Aeon Technology Co., Ltd.
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