eudamed_udi
Primary ID: 03665155000809
ERGOTECH BEIGE (UDI 03665155000809)
Manufactured by FDI FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ERGOTECH BEIGE - Primary ID 03665155000809
Device Regulatory Overview
The ERGOTECH BEIGE (Model/Catalog Number: ET/01/08) 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/01/08
- Product Code / EMDN
- Y12030602
- Device Name
- Canne anglaise
- Database Sync Date
- 2026-08-09 16:59:59
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ERGOTECH BEIGE?
The registered manufacturer of record for ERGOTECH BEIGE is FDI FRANCE.
What is the Primary UDI-DI identifier for ERGOTECH BEIGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665155000809.
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
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