GUDIDData
eudamed_udi Primary ID: 00842768006692

N Latex IgG4 (UDI 00842768006692)

Manufactured by Siemens Healthcare Diagnostics Products GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N Latex IgG4 - Primary ID 00842768006692

Device Regulatory Overview

The N Latex IgG4 (Model/Catalog Number: 10445971) is a medical device manufactured by Siemens Healthcare Diagnostics Products GmbH. This product is indexed under FDA Product Code / Category Classification W0102010106 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10445971
Product Code / EMDN
W0102010106
Device Name
IVDR_27_MAR EB_B_REAG_N_La_IGG4
Database Sync Date
2026-08-09 16:29:21

Full Regulatory Attributes

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{
    "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 N Latex IgG4?

The registered manufacturer of record for N Latex IgG4 is Siemens Healthcare Diagnostics Products GmbH.

What is the Primary UDI-DI identifier for N Latex IgG4?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00842768006692.

What classification code is assigned to this device?

This device is registered under product classification code W0102010106.

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