GUDIDData
gudid Primary ID: 90T0015

ScaleOR (UDI 90T0015)

Manufactured by Nds Surgical Imaging LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ScaleOR - Primary ID 90T0015

Device Regulatory Overview

The ScaleOR (Model/Catalog Number: 90T0015) is a medical device manufactured by Nds Surgical Imaging LLC. This product is indexed under FDA Product Code / Category Classification LMD within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
90T0015
Product Code / EMDN
LMD
Device Name
ScaleOR, S-Video/Comp Input, W/O Fiber, ND-00B-014/0
Database Sync Date
2026-08-09 09:32:54

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 ScaleOR?

The registered manufacturer of record for ScaleOR is Nds Surgical Imaging LLC.

What is the Primary UDI-DI identifier for ScaleOR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90T0015.

What classification code is assigned to this device?

This device is registered under product classification code LMD.

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