gudid
Primary ID: C52900
UA Win10 Kit (UDI C52900)
Manufactured by BECKMAN COULTER IRELAND INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UA Win10 Kit - Primary ID C52900
Device Regulatory Overview
The UA Win10 Kit (Model/Catalog Number: C52900) is a medical device manufactured by BECKMAN COULTER IRELAND INC.. This product is indexed under FDA Product Code / Category Classification KQO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C52900
- Product Code / EMDN
- KQO
- Device Name
- Urinalysis Win10 Kit with PC7 hardware
- Database Sync Date
- 2026-08-09 09:22:50
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 UA Win10 Kit?
The registered manufacturer of record for UA Win10 Kit is BECKMAN COULTER IRELAND INC..
What is the Primary UDI-DI identifier for UA Win10 Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C52900.
What classification code is assigned to this device?
This device is registered under product classification code KQO.
Similar Classification Devices (KQO)
Other Devices by BECKMAN COULTER IRELAND INC.
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