gudid Primary ID: 1342/A2/F

KENEX (UDI 1342/A2/F)

Manufactured by KENEX (ELECTRO-MEDICAL) LIMITED

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

Scannable UDI-DI Representation

Device Regulatory Overview

The KENEX (Model/Catalog Number: 1342/A2/F) is a medical device manufactured by KENEX (ELECTRO-MEDICAL) LIMITED. This product is indexed under FDA Product Code / Category Classification KPY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1342/A2/F
Product Code / EMDN: KPY
Device Name: Mobile St. Cart - Table shield x2 & Top shield x2
Database Sync Date: 2026-08-09 09:08:20

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 KENEX?

The registered manufacturer of record for KENEX is KENEX (ELECTRO-MEDICAL) LIMITED.

What is the Primary UDI-DI identifier for KENEX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1342/A2/F.

What classification code is assigned to this device?

This device is registered under product classification code KPY.

Similar Classification Devices (KPY)

Other Devices by KENEX (ELECTRO-MEDICAL) LIMITED

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