gudid
Primary ID: 510395
DailyChek QC Kit (UDI 510395)
Manufactured by American National Red Cross
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DailyChek QC Kit - Primary ID 510395
Device Regulatory Overview
The DailyChek QC Kit (Model/Catalog Number: 510395) is a medical device manufactured by American National Red Cross. This product is indexed under FDA Product Code / Category Classification KSF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 510395
- Product Code / EMDN
- KSF
- Device Name
- Blood Bank kit used to perform quality control testing of reverse grouping and screening cell reagent red blood cells.
- Database Sync Date
- 2026-08-09 09:49:26
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 DailyChek QC Kit?
The registered manufacturer of record for DailyChek QC Kit is American National Red Cross.
What is the Primary UDI-DI identifier for DailyChek QC Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 510395.
What classification code is assigned to this device?
This device is registered under product classification code KSF.
Similar Classification Devices (KSF)
Other Devices by American National Red Cross
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