GUDIDData
eudamed_udi Primary ID: B941204040

KineQuantum Wireless (UDI B941204040)

Manufactured by KineQuantum

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KineQuantum Wireless - Primary ID B941204040

Device Regulatory Overview

The KineQuantum Wireless (Model/Catalog Number: 20404) is a medical device manufactured by KineQuantum. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
20404
Product Code / EMDN
Z12069099
Device Name
KQSOFT
Database Sync Date
2026-08-09 16:29:18

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 KineQuantum Wireless?

The registered manufacturer of record for KineQuantum Wireless is KineQuantum.

What is the Primary UDI-DI identifier for KineQuantum Wireless?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B941204040.

What classification code is assigned to this device?

This device is registered under product classification code Z12069099.

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