eudamed_udi
Primary ID: 06970742221435
DR HO'S (UDI 06970742221435)
Manufactured by Guangzhou Xinbo Electronic Co.,Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DR HO'S - Primary ID 06970742221435
Device Regulatory Overview
The DR HO'S (Model/Catalog Number: 143) is a medical device manufactured by Guangzhou Xinbo Electronic 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
- 143
- Product Code / EMDN
- Z12062801
- Device Name
- Neck Pain Pro
- Database Sync Date
- 2026-08-09 16:46:38
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 DR HO'S?
The registered manufacturer of record for DR HO'S is Guangzhou Xinbo Electronic Co.,Ltd.
What is the Primary UDI-DI identifier for DR HO'S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970742221435.
What classification code is assigned to this device?
This device is registered under product classification code Z12062801.
Similar Classification Devices (Z12062801)
Other Devices by Guangzhou Xinbo Electronic Co.,Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint