eudamed_udi
Primary ID: 03665155001080
TRIPOD (UDI 03665155001080)
Manufactured by FDI FRANCE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRIPOD - Primary ID 03665155001080
Device Regulatory Overview
The TRIPOD (Model/Catalog Number: TR/05/07) is a medical device manufactured by FDI FRANCE. This product is indexed under FDA Product Code / Category Classification Y120315 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TR/05/07
- Product Code / EMDN
- Y120315
- Device Name
- TRIPOD
- Database Sync Date
- 2026-08-09 16:51:17
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 TRIPOD?
The registered manufacturer of record for TRIPOD is FDI FRANCE.
What is the Primary UDI-DI identifier for TRIPOD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03665155001080.
What classification code is assigned to this device?
This device is registered under product classification code Y120315.
Similar Classification Devices (Y120315)
Other Devices by FDI FRANCE
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