eudamed_udi Primary ID: 00606959055704

Trilogy Evo, O2, Turkey (UDI 00606959055704)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Trilogy Evo, O2, Turkey (Model/Catalog Number: TR2100X15B) is a medical device manufactured by Respironics Inc.. This product is indexed under FDA Product Code / Category Classification Z12030103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TR2100X15B
Product Code / EMDN: Z12030103
Device Name: Trilogy Evo, O2, Turkey
Database Sync Date: 2026-08-09 16:29:16

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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Frequently Asked Questions

Who is the primary manufacturer of Trilogy Evo, O2, Turkey?

The registered manufacturer of record for Trilogy Evo, O2, Turkey is Respironics Inc..

What is the Primary UDI-DI identifier for Trilogy Evo, O2, Turkey?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00606959055704.

What classification code is assigned to this device?

This device is registered under product classification code Z12030103.

Similar Classification Devices (Z12030103)

Other Devices by Respironics Inc.

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