eudamed_udi
Primary ID: B941201020
KineQuantum éco (UDI B941201020)
Manufactured by KineQuantum
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KineQuantum éco - Primary ID B941201020
Device Regulatory Overview
The KineQuantum éco (Model/Catalog Number: 20102) 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
- 20102
- Product Code / EMDN
- Z12069099
- Device Name
- KQSOFT
- Database Sync Date
- 2026-08-09 16:48:55
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 éco?
The registered manufacturer of record for KineQuantum éco is KineQuantum.
What is the Primary UDI-DI identifier for KineQuantum éco?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is B941201020.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
Similar Classification Devices (Z12069099)
Other Devices by KineQuantum
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