gudid
Primary ID: 382940-REG
Regard (UDI 382940-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 382940-REG
Device Regulatory Overview
The Regard (Model/Catalog Number: 382940-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
- 382940-REG
- Product Code / EMDN
- FMR
- Device Name
- Pocket Slide-Lateral Transfer Tube-Disposable 36X40
- 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 382940-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