eudamed_udi
Primary ID: 03665155000229
ERGOTECH WHITE (UDI 03665155000229)
Manufactured by FDI FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERGOTECH WHITE - Primary ID 03665155000229
Device Regulatory Overview
The ERGOTECH WHITE (Model/Catalog Number: ET/05/06) is a medical device manufactured by FDI FRANCE. This product is indexed under FDA Product Code / Category Classification Y12030602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ET/05/06
- Product Code / EMDN
- Y12030602
- Device Name
- Canne anglaise
- Database Sync Date
- 2026-08-09 17:18:55
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 ERGOTECH WHITE?
The registered manufacturer of record for ERGOTECH WHITE is FDI FRANCE.
What is the Primary UDI-DI identifier for ERGOTECH WHITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665155000229.
What classification code is assigned to this device?
This device is registered under product classification code Y12030602.
Similar Classification Devices (Y12030602)
Other Devices by FDI FRANCE
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint