gudid
Primary ID: L950
Leander (UDI L950)
Manufactured by Leander, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Leander - Primary ID L950
Device Regulatory Overview
The Leander (Model/Catalog Number: L950) is a medical device manufactured by Leander, LLC. This product is indexed under FDA Product Code / Category Classification LGX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- L950
- Product Code / EMDN
- LGX
- Device Name
- Examination/treatment motorized table with some articulated sections that can be adjusted into various accommodations for patient comfort and/or treatment. It is typically used by physical therapists and chiropractors.
- Database Sync Date
- 2026-08-09 09:03:51
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 Leander?
The registered manufacturer of record for Leander is Leander, LLC.
What is the Primary UDI-DI identifier for Leander?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L950.
What classification code is assigned to this device?
This device is registered under product classification code LGX.
Similar Classification Devices (LGX)
Other Devices by Leander, LLC
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