GUDIDData
gudid Primary ID: 0066907

Capture-R Ready Indicator Red Cells (UDI 0066907)

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 Indicator Red Cells - Primary ID 0066907

Device Regulatory Overview

The Capture-R Ready Indicator Red Cells (Model/Catalog Number: 0066907) is a medical device manufactured by IMMUCOR, INC.. This product is indexed under FDA Product Code / Category Classification KSF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
0066907
Product Code / EMDN
KSF
Device Name
Anti-IgG-coated Indicator Red Cells for use in Capture-R Ready-Screen, Capture-R Ready-ID or Capture-R Select Solid Phase Assays for the detection of IgG antibodies to red blood cells.
Database Sync Date
2026-08-09 09:39:01

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Capture-R Ready Indicator Red Cells?

The registered manufacturer of record for Capture-R Ready Indicator Red Cells is IMMUCOR, INC..

What is the Primary UDI-DI identifier for Capture-R Ready Indicator Red Cells?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0066907.

What classification code is assigned to this device?

This device is registered under product classification code KSF.

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