eudamed_udi
Primary ID: B941202070
KineQuantum Pro (UDI B941202070)
Manufactured by KineQuantum
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KineQuantum Pro - Primary ID B941202070
Device Regulatory Overview
The KineQuantum Pro (Model/Catalog Number: 20207) 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
- 20207
- Product Code / EMDN
- Z12069099
- Device Name
- KQSOFT
- Database Sync Date
- 2026-08-09 17:19:32
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 KineQuantum Pro?
The registered manufacturer of record for KineQuantum Pro is KineQuantum.
What is the Primary UDI-DI identifier for KineQuantum Pro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B941202070.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
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Other Devices by KineQuantum
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