gudid
Primary ID: XB430
Senolo (UDI XB430)
Manufactured by JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Senolo - Primary ID XB430
Device Regulatory Overview
The Senolo (Model/Catalog Number: XB430) is a medical device manufactured by JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD.. This product is indexed under FDA Product Code / Category Classification HSP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- XB430
- Product Code / EMDN
- HSP
- Device Name
- Database Sync Date
- 2026-08-09 09:21:59
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 Senolo?
The registered manufacturer of record for Senolo is JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD..
What is the Primary UDI-DI identifier for Senolo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is XB430.
What classification code is assigned to this device?
This device is registered under product classification code HSP.
Similar Classification Devices (HSP)
Other Devices by JIANGSU SENOLO MEDICAL TECHNOLOGY CO., LTD.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint