GUDIDData
gudid Primary ID: X-Large

Viscera Retainer Radiopaque Center Spine (UDI X-Large)

Manufactured by RAINBOW MEDICAL DEVICES LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Viscera Retainer Radiopaque Center Spine - Primary ID X-Large

Device Regulatory Overview

The Viscera Retainer Radiopaque Center Spine (Model/Catalog Number: X-Large) is a medical device manufactured by RAINBOW MEDICAL DEVICES LLC. This product is indexed under FDA Product Code / Category Classification GCZ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
X-Large
Product Code / EMDN
GCZ
Device Name
One unit packaged in a Poly/Poly Chevron sealed pouch, Gama Sterilized with a 3 year shelf life. The Viscera Retainer is made up of green plastic and is flat on one side with ribs on the other to support placement in viscera region with a over molded radiopaque center spine up the middle of the unit for additional support for placement and extraction. The retainer has an attached pull cord and ring for easy removal when suturing is about complete.
Database Sync Date
2026-08-09 09:49:27

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 Viscera Retainer Radiopaque Center Spine?

The registered manufacturer of record for Viscera Retainer Radiopaque Center Spine is RAINBOW MEDICAL DEVICES LLC.

What is the Primary UDI-DI identifier for Viscera Retainer Radiopaque Center Spine?

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

What classification code is assigned to this device?

This device is registered under product classification code GCZ.

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