GUDIDData
gudid Primary ID: 10873929

INNOVANCE Heparin LMW Control 1 (UDI 10873929)

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 INNOVANCE Heparin LMW Control 1 - Primary ID 10873929

Device Regulatory Overview

The INNOVANCE Heparin LMW Control 1 (Model/Catalog Number: 10873929) is a medical device manufactured by Siemens Healthcare Diagnostics Products GmbH. This product is indexed under FDA Product Code / Category Classification GGN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10873929
Product Code / EMDN
GGN
Device Name
For quality control of the INNOVANCE Heparin assay
Database Sync Date
2026-08-09 09:32:41

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 INNOVANCE Heparin LMW Control 1?

The registered manufacturer of record for INNOVANCE Heparin LMW Control 1 is Siemens Healthcare Diagnostics Products GmbH.

What is the Primary UDI-DI identifier for INNOVANCE Heparin LMW Control 1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10873929.

What classification code is assigned to this device?

This device is registered under product classification code GGN.

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