gudid
Primary ID: 90T0022
ExpandOR (UDI 90T0022)
Manufactured by Nds Surgical Imaging LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ExpandOR - Primary ID 90T0022
Device Regulatory Overview
The ExpandOR (Model/Catalog Number: 90T0022) 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
- 90T0022
- Product Code / EMDN
- LMD
- Device Name
- ExpandOR, DVI, Audio, ND-00B-R17/0
- Database Sync Date
- 2026-08-09 09:32:54
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ExpandOR?
The registered manufacturer of record for ExpandOR is Nds Surgical Imaging LLC.
What is the Primary UDI-DI identifier for ExpandOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90T0022.
What classification code is assigned to this device?
This device is registered under product classification code LMD.
Similar Classification Devices (LMD)
Other Devices by Nds Surgical Imaging LLC
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