gudid
Primary ID: 1350/1
KENEX (UDI 1350/1)
Manufactured by KENEX (ELECTRO-MEDICAL) LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KENEX - Primary ID 1350/1
Device Regulatory Overview
The KENEX (Model/Catalog Number: 1350/1) is a medical device manufactured by KENEX (ELECTRO-MEDICAL) LIMITED. This product is indexed under FDA Product Code / Category Classification IXA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1350/1
- Product Code / EMDN
- IXA
- Device Name
- 1350/1 Mobile Tube Head with Detector Holder
- 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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Get API Token Access ($49/mo)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 1350/1.
What classification code is assigned to this device?
This device is registered under product classification code IXA.
Similar Classification Devices (IXA)
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