gudid
Primary ID: 0006420
Capture LISS (UDI 0006420)
Manufactured by IMMUCOR, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Capture LISS - Primary ID 0006420
Device Regulatory Overview
The Capture LISS (Model/Catalog Number: 0006420) 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
- 0006420
- Product Code / EMDN
- KSS
- Device Name
- Capture LISS is for use as a low ionic strength potentiator and sample addition indicator in Capture solid phase tests for the detection of antibodies. This product is the 11.5 mL vial version with ten vials packaged.
- Database Sync Date
- 2026-08-09 09:39:02
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 LISS?
The registered manufacturer of record for Capture LISS is IMMUCOR, INC..
What is the Primary UDI-DI identifier for Capture LISS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0006420.
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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