FORTIS6002/HCT-9123Champagne (UDI 06973536540668)
Manufactured by Foshan HCT Medical Equipment Co.,ltd
Device Regulatory Overview
The FORTIS6002/HCT-9123Champagne (Model/Catalog Number: 60021439/HCT-9123Champagne) is a medical device manufactured by Foshan HCT Medical Equipment Co.,ltd. This product is indexed under FDA Product Code / Category Classification Y120612 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 60021439/HCT-9123Champagne
- Product Code / EMDN
- Y120612
- Device Name
- rollator
- Database Sync Date
- 2026-08-09 16:28:54
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 FORTIS6002/HCT-9123Champagne?
The registered manufacturer of record for FORTIS6002/HCT-9123Champagne is Foshan HCT Medical Equipment Co.,ltd.
What is the Primary UDI-DI identifier for FORTIS6002/HCT-9123Champagne?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973536540668.
What classification code is assigned to this device?
This device is registered under product classification code Y120612.
Similar Classification Devices (Y120612)
Other Devices by Foshan HCT Medical Equipment Co.,ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint