GUDIDData
gudid Primary ID: 10445163

Dimension Vista Flex reagent cartridge CO2 (UDI 10445163)

Manufactured by Siemens Healthcare Diagnostics Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dimension Vista Flex reagent cartridge CO2 - Primary ID 10445163

Device Regulatory Overview

The Dimension Vista Flex reagent cartridge CO2 (Model/Catalog Number: 10445163) is a medical device manufactured by Siemens Healthcare Diagnostics Inc.. This product is indexed under FDA Product Code / Category Classification KHS 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-2087-2016 View Full Alert →

Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module (10703032 or 10713761) ...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-2058-2014 View Full Alert →

Coat-A-Count Direct Androstenedione, SMN 10381049, Catalog Number TKAN1. Siemens Healthcare Diagnostics...

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ID: Z-0459-2016 View Full Alert →

Reagent Management System (RMS) Dimension EXL with LM STM Product Usage: The Reagent Management System (RMS) is a module for use with ...

🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
10445163
Product Code / EMDN
KHS
Device Name
Carbon Dioxide Flex reagent cartridge, 3360 Tests
Database Sync Date
2026-08-09 09:13:52

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 Dimension Vista Flex reagent cartridge CO2?

The registered manufacturer of record for Dimension Vista Flex reagent cartridge CO2 is Siemens Healthcare Diagnostics Inc..

What is the Primary UDI-DI identifier for Dimension Vista Flex reagent cartridge CO2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10445163.

What classification code is assigned to this device?

This device is registered under product classification code KHS.

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