GUDIDData
gudid Primary ID: 10381447

IMMULITE 2000 Systems IGFBP-3 (UDI 10381447)

Manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IMMULITE 2000 Systems IGFBP-3 - Primary ID 10381447

Device Regulatory Overview

The IMMULITE 2000 Systems IGFBP-3 (Model/Catalog Number: 10381447) is a medical device manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD. This product is indexed under FDA Product Code / Category Classification CFL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10381447
Product Code / EMDN
CFL
Device Name
IGF BP3 - IMMULITE - RGT - 200 Tests
Database Sync Date
2026-08-09 09:32:40

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 IMMULITE 2000 Systems IGFBP-3?

The registered manufacturer of record for IMMULITE 2000 Systems IGFBP-3 is SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD.

What is the Primary UDI-DI identifier for IMMULITE 2000 Systems IGFBP-3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10381447.

What classification code is assigned to this device?

This device is registered under product classification code CFL.

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