GUDIDData
gudid Primary ID: XB336

Senolo (UDI XB336)

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 XB336

Device Regulatory Overview

The Senolo (Model/Catalog Number: XB336) 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
XB336
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
}
                            

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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 XB336.

What classification code is assigned to this device?

This device is registered under product classification code HSP.

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