gudid
Primary ID: 0066204
Capture-R Ready-ID (UDI 0066204)
Manufactured by IMMUCOR, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Capture-R Ready-ID - Primary ID 0066204
Device Regulatory Overview
The Capture-R Ready-ID (Model/Catalog Number: 0066204) is a medical device manufactured by IMMUCOR, INC.. This product is indexed under FDA Product Code / Category Classification within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0066204
- Product Code / EMDN
- N/A
- Device Name
- Capture-R Ready-ID is used in the detection and identification of unexpected IgG antibodies to red blood cells by manual, semi-automated or automated solid phase red blood cell adherence methods. This product is a double-strip configuration which carry the bound and dried membranes prepared from 14 group O donors. Each microplate contains six (6) double-strips, and the plate is sealed in a pouch.
- 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-R Ready-ID?
The registered manufacturer of record for Capture-R Ready-ID is IMMUCOR, INC..
What is the Primary UDI-DI identifier for Capture-R Ready-ID?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0066204.
What classification code is assigned to this device?
This device is registered under product classification code .
Similar Classification Devices ()
Other Devices by IMMUCOR, INC.
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