GUDIDData
eudamed_udi Primary ID: 29556564089692

Medline (UDI 29556564089692)

Manufactured by Karex Industries Sdn. Bhd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Medline - Primary ID 29556564089692

Device Regulatory Overview

The Medline (Model/Catalog Number: KX07) is a medical device manufactured by Karex Industries Sdn. Bhd.. This product is indexed under FDA Product Code / Category Classification Z11040185 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KX07
Product Code / EMDN
Z11040185
Device Name
Non-Sterile Natural Rubber Latex Protective Transducer Covers
Database Sync Date
2026-08-09 16:48:03

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Medline?

The registered manufacturer of record for Medline is Karex Industries Sdn. Bhd..

What is the Primary UDI-DI identifier for Medline?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 29556564089692.

What classification code is assigned to this device?

This device is registered under product classification code Z11040185.

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