Capture-P Positive Control Serum (Weak), Capture-P Negative Control Serum (UDI 0066905)
Manufactured by IMMUCOR, INC.
Device Regulatory Overview
The Capture-P Positive Control Serum (Weak), Capture-P Negative Control Serum (Model/Catalog Number: 0066905) is a medical device manufactured by IMMUCOR, INC.. This product is indexed under FDA Product Code / Category Classification KSS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0066905
- Product Code / EMDN
- KSS
- Device Name
- Immucors Capture-P Positive Control Serum (Weak) and Capture-P Negative Control Serum are run controls to be used in the Capture-P and Capture-P Ready-Screen Solid Phase assays.
- Database Sync Date
- 2026-08-09 09:39:01
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 Capture-P Positive Control Serum (Weak), Capture-P Negative Control Serum?
The registered manufacturer of record for Capture-P Positive Control Serum (Weak), Capture-P Negative Control Serum is IMMUCOR, INC..
What is the Primary UDI-DI identifier for Capture-P Positive Control Serum (Weak), Capture-P Negative Control Serum?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0066905.
What classification code is assigned to this device?
This device is registered under product classification code KSS.
Similar Classification Devices (KSS)
Other Devices by IMMUCOR, INC.
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