eudamed_udi
Primary ID: 00606959051959
Trilogy Evo, International (UDI 00606959051959)
Manufactured by Respironics Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Trilogy Evo, International - Primary ID 00606959051959
Device Regulatory Overview
The Trilogy Evo, International (Model/Catalog Number: IN2110X15B) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification Z12030104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IN2110X15B
- Product Code / EMDN
- Z12030104
- Device Name
- Trilogy Evo, International
- Database Sync Date
- 2026-08-09 16:29:03
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 Trilogy Evo, International?
The registered manufacturer of record for Trilogy Evo, International is Respironics Inc..
What is the Primary UDI-DI identifier for Trilogy Evo, International?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959051959.
What classification code is assigned to this device?
This device is registered under product classification code Z12030104.
Similar Classification Devices (Z12030104)
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