GUDIDData
gudid Primary ID: Bright Orange - Headrail

NeoHug (UDI Bright Orange - Headrail)

Manufactured by Neotech Products LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NeoHug - Primary ID Bright Orange - Headrail

Device Regulatory Overview

The NeoHug (Model/Catalog Number: Bright Orange - Headrail) is a medical device manufactured by Neotech Products LLC. This product is indexed under FDA Product Code / Category Classification JAY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Bright Orange - Headrail
Product Code / EMDN
JAY
Device Name
NeoHug is intended to support, organize or hold non-operating medical devices.
Database Sync Date
2026-08-09 09:46:41

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 NeoHug?

The registered manufacturer of record for NeoHug is Neotech Products LLC.

What is the Primary UDI-DI identifier for NeoHug?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Bright Orange - Headrail.

What classification code is assigned to this device?

This device is registered under product classification code JAY.

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