GUDIDData
gudid Primary ID: SLIDESTD-REG

Regard (UDI SLIDESTD-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 SLIDESTD-REG

Device Regulatory Overview

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

Technical Specifications

Model Number
SLIDESTD-REG
Product Code / EMDN
FMR
Device Name
Slide Transfer Tube 58"x29" Orange
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
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 SLIDESTD-REG.

What classification code is assigned to this device?

This device is registered under product classification code FMR.

Similar Classification Devices (FMR)

Other Devices by Resource Optimization & Innovation, L.L.C.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint