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gudid Primary ID: 11306490

ADVIA 120/2120/2120i Aspiration Pathway Wash Kit (UDI 11306490)

Manufactured by Siemens Healthcare Diagnostics Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ADVIA 120/2120/2120i Aspiration Pathway Wash Kit - Primary ID 11306490

Device Regulatory Overview

The ADVIA 120/2120/2120i Aspiration Pathway Wash Kit (Model/Catalog Number: 11306490) is a medical device manufactured by Siemens Healthcare Diagnostics Inc.. This product is indexed under FDA Product Code / Category Classification JCB 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) ...

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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
11306490
Product Code / EMDN
JCB
Device Name
ADVIA 120/2120/2120i Aspiration Pathway Wash Kit
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 ADVIA 120/2120/2120i Aspiration Pathway Wash Kit?

The registered manufacturer of record for ADVIA 120/2120/2120i Aspiration Pathway Wash Kit is Siemens Healthcare Diagnostics Inc..

What is the Primary UDI-DI identifier for ADVIA 120/2120/2120i Aspiration Pathway Wash Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11306490.

What classification code is assigned to this device?

This device is registered under product classification code JCB.

Similar Classification Devices (JCB)

Other Devices by Siemens Healthcare Diagnostics Inc.

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