GUDIDData
gudid Primary ID: FG1-A4-000060

RIVA Posterior Fixation System (UDI FG1-A4-000060)

Manufactured by XENIX MEDICAL LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RIVA Posterior Fixation System - Primary ID FG1-A4-000060

Device Regulatory Overview

The RIVA Posterior Fixation System (Model/Catalog Number: FG1-A4-000060) is a medical device manufactured by XENIX MEDICAL LLC. This product is indexed under FDA Product Code / Category Classification HWN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FG1-A4-000060
Product Code / EMDN
HWN
Device Name
Compressor
Database Sync Date
2026-08-09 09:08:44

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 RIVA Posterior Fixation System?

The registered manufacturer of record for RIVA Posterior Fixation System is XENIX MEDICAL LLC.

What is the Primary UDI-DI identifier for RIVA Posterior Fixation System?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FG1-A4-000060.

What classification code is assigned to this device?

This device is registered under product classification code HWN.

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