GUDIDData
eudamed_udi Primary ID: 00630414240367

INNOVANCE Rivaroxaban Standards (UDI 00630414240367)

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 Rivaroxaban Standards - Primary ID 00630414240367

Device Regulatory Overview

The INNOVANCE Rivaroxaban Standards (Model/Catalog Number: 10873677) is a medical device manufactured by Siemens Healthcare Diagnostics Products GmbH. This product is indexed under FDA Product Code / Category Classification W0103020701 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
10873677
Product Code / EMDN
W0103020701
Device Name
IVDR_27_MAR EB_C_INN_Riva_Stand
Database Sync Date
2026-08-09 16:29:41

Full Regulatory Attributes

πŸ”’ 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 INNOVANCE Rivaroxaban Standards?

The registered manufacturer of record for INNOVANCE Rivaroxaban Standards is Siemens Healthcare Diagnostics Products GmbH.

What is the Primary UDI-DI identifier for INNOVANCE Rivaroxaban Standards?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00630414240367.

What classification code is assigned to this device?

This device is registered under product classification code W0103020701.

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