GUDIDData
eudamed_udi Primary ID: 15099590749743

MicroScan Neg Urine Combo 95 (UDI 15099590749743)

Manufactured by Beckman Coulter Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MicroScan Neg Urine Combo 95 - Primary ID 15099590749743

Device Regulatory Overview

The MicroScan Neg Urine Combo 95 (Model/Catalog Number: C79387) is a medical device manufactured by Beckman Coulter Inc.. This product is indexed under FDA Product Code / Category Classification W0203010185 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.

ID: Z-0071-2026 View Full Alert →

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ID: Z-0441-2026 View Full Alert →

SYNCHRON Systems Direct LDL Cholesterol (LDLD) Reagent, REF: 969706...

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ID: Z-0032-2026 View Full Alert →

DxC 500 AU Module w/ISE, DxC 500i, With ISE, REF: C63522 and DxC 500 AU Module, DxC 500i, Without ISE, REF: C6352; part of the DxC 500i Clin...

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Technical Specifications

Model Number
C79387
Product Code / EMDN
W0203010185
Device Name
MicroScan Neg MIC/Combo Panel Family
Database Sync Date
2026-08-09 17:46:09

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 MicroScan Neg Urine Combo 95?

The registered manufacturer of record for MicroScan Neg Urine Combo 95 is Beckman Coulter Inc..

What is the Primary UDI-DI identifier for MicroScan Neg Urine Combo 95?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15099590749743.

What classification code is assigned to this device?

This device is registered under product classification code W0203010185.

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