GUDIDData
eudamed_udi Primary ID: 06941691973386

Patient Cable (UDI 06941691973386)

Manufactured by Orantech Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Patient Cable - Primary ID 06941691973386

Device Regulatory Overview

The Patient Cable (Model/Catalog Number: FM-05) is a medical device manufactured by Orantech Inc.. This product is indexed under FDA Product Code / Category Classification Z1203020285 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FM-05
Product Code / EMDN
Z1203020285
Device Name
Patient Cable
Database Sync Date
2026-08-09 16:28:44

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 Patient Cable?

The registered manufacturer of record for Patient Cable is Orantech Inc..

What is the Primary UDI-DI identifier for Patient Cable?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06941691973386.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020285.

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