eudamed_udi
Primary ID: 08057509262370
Tripode (UDI 08057509262370)
Manufactured by IDS S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tripode - Primary ID 08057509262370
Device Regulatory Overview
The Tripode (Model/Catalog Number: ID-KL5407) is a medical device manufactured by IDS S.r.l.. This product is indexed under FDA Product Code / Category Classification Y120315 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ID-KL5407
- Product Code / EMDN
- Y120315
- Device Name
- Tripode
- Database Sync Date
- 2026-08-09 17:02:22
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 Tripode?
The registered manufacturer of record for Tripode is IDS S.r.l..
What is the Primary UDI-DI identifier for Tripode?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057509262370.
What classification code is assigned to this device?
This device is registered under product classification code Y120315.
Similar Classification Devices (Y120315)
Other Devices by IDS S.r.l.
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