gudid Primary ID: GUDID-fcda005db3

Inion GTR instrument (UDI GUDID-fcda005db3)

Manufactured by Inion Oy

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Inion GTR instrument (Model/Catalog Number: Unspecified) is a medical device manufactured by Inion Oy. This product is indexed under FDA Product Code / Category Classification NPK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N/A
Product Code / EMDN: NPK
Device Name: Re-usable tack applicator
Database Sync Date: 2026-08-09 09:14:43

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 Inion GTR instrument?

The registered manufacturer of record for Inion GTR instrument is Inion Oy.

What is the Primary UDI-DI identifier for Inion GTR instrument?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GUDID-fcda005db3.

What classification code is assigned to this device?

This device is registered under product classification code NPK.

Similar Classification Devices (NPK)

Other Devices by Inion Oy

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