NA (UDI TAB800KT)

Manufactured by STERIS

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: TAB800KT) is a medical device manufactured by STERIS. This product is indexed under FDA Product Code / Category Classification GDC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: TAB800KT
Product Code / EMDN: GDC
Device Name: Catheter extension is used with the CMAX X-Ray Imaging Table
Database Sync Date: 2026-08-09 09:19:08

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 NA?

The registered manufacturer of record for NA is STERIS.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TAB800KT.

What classification code is assigned to this device?

This device is registered under product classification code GDC.

Similar Classification Devices (GDC)

Other Devices by STERIS

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