gudid
Primary ID: Face Fitness
Tua (UDI Face Fitness)
Manufactured by VUPIESSE SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tua - Primary ID Face Fitness
Device Regulatory Overview
The Tua (Model/Catalog Number: Face Fitness) is a medical device manufactured by VUPIESSE SRL. This product is indexed under FDA Product Code / Category Classification NFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Face Fitness
- Product Code / EMDN
- NFO
- Device Name
- Facial stimulator indicated for over the counter cosmetic use.
- Database Sync Date
- 2026-08-09 09:05:06
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 Tua?
The registered manufacturer of record for Tua is VUPIESSE SRL.
What is the Primary UDI-DI identifier for Tua?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Face Fitness.
What classification code is assigned to this device?
This device is registered under product classification code NFO.
Similar Classification Devices (NFO)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint