ORTHO Daily QC Simulated Whole Blood Quality Control Kit (UDI 6708858)
Manufactured by MILLIPORE (U.K.) LIMITED
Device Regulatory Overview
The ORTHO Daily QC Simulated Whole Blood Quality Control Kit (Model/Catalog Number: 6708858) is a medical device manufactured by MILLIPORE (U.K.) LIMITED. This product is indexed under FDA Product Code / Category Classification KSF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 6708858
- Product Code / EMDN
- KSF
- Device Name
- Database Sync Date
- 2026-08-09 09:11:42
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 ORTHO Daily QC Simulated Whole Blood Quality Control Kit?
The registered manufacturer of record for ORTHO Daily QC Simulated Whole Blood Quality Control Kit is MILLIPORE (U.K.) LIMITED.
What is the Primary UDI-DI identifier for ORTHO Daily QC Simulated Whole Blood Quality Control Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6708858.
What classification code is assigned to this device?
This device is registered under product classification code KSF.
Similar Classification Devices (KSF)
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