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enforcement Primary ID: Z-2264-2025

UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205, (UDI Z-2264-2025)

Manufactured by Beckman Coulter Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205, - Primary ID Z-2264-2025

Device Regulatory Overview

The UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205, (Model/Catalog Number: Unspecified) is a medical device manufactured by Beckman Coulter Inc.. This product is indexed under FDA Product Code / Category Classification All Lots/(01)15099590011925 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

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Technical Specifications

Model Number
N/A
Product Code / EMDN
All Lots/(01)15099590011925
Device Name
UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205,
Database Sync Date
2026-08-09 10:06:32

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 UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205,?

The registered manufacturer of record for UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205, is Beckman Coulter Inc..

What is the Primary UDI-DI identifier for UIBC (Unsaturated Iron Binding Capacity), REF: OSR61205,?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-2264-2025.

What classification code is assigned to this device?

This device is registered under product classification code All Lots/(01)15099590011925.

Other Devices by Beckman Coulter Inc.

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