GUDIDData
gudid Primary ID: CVRBTTIEL-REG

Regard (UDI CVRBTTIEL-REG)

Manufactured by Resource Optimization & Innovation, L.L.C.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Regard - Primary ID CVRBTTIEL-REG

Device Regulatory Overview

The Regard (Model/Catalog Number: CVRBTTIEL-REG) is a medical device manufactured by Resource Optimization & Innovation, L.L.C.. This product is indexed under FDA Product Code / Category Classification FXP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
CVRBTTIEL-REG
Product Code / EMDN
FXP
Device Name
COVER BOOT FLD RST REGULAR LARGE FOM NON SKD CTD PP BLUE
Database Sync Date
2026-08-09 09:20:10

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 Regard?

The registered manufacturer of record for Regard is Resource Optimization & Innovation, L.L.C..

What is the Primary UDI-DI identifier for Regard?

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

What classification code is assigned to this device?

This device is registered under product classification code FXP.

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