gudid Primary ID: K123659-00-1705-D

UniTip High Resolution Catheter (UDI K123659-00-1705-D)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The UniTip High Resolution Catheter (Model/Catalog Number: K123659-00-1705-D) is a medical device manufactured by Unisensor AG. This product is indexed under FDA Product Code / Category Classification FFX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: K123659-00-1705-D
Product Code / EMDN: FFX
Device Name
Database Sync Date: 2026-08-09 09:16:10

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 UniTip High Resolution Catheter?

The registered manufacturer of record for UniTip High Resolution Catheter is Unisensor AG.

What is the Primary UDI-DI identifier for UniTip High Resolution Catheter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is K123659-00-1705-D.

What classification code is assigned to this device?

This device is registered under product classification code FFX.

Similar Classification Devices (FFX)

Other Devices by Unisensor AG

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