gudid
Primary ID: 48
PAT-LRT (UDI 48)
Manufactured by Nu Dimension Tech Ventures LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PAT-LRT - Primary ID 48
Device Regulatory Overview
The PAT-LRT (Model/Catalog Number: 48) is a medical device manufactured by Nu Dimension Tech Ventures LLC. This product is indexed under FDA Product Code / Category Classification FNM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 48
- Product Code / EMDN
- FNM
- Device Name
- Low Airloss Rotational Air Mattress 48 inch
- 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 PAT-LRT?
The registered manufacturer of record for PAT-LRT is Nu Dimension Tech Ventures LLC.
What is the Primary UDI-DI identifier for PAT-LRT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 48.
What classification code is assigned to this device?
This device is registered under product classification code FNM.
Similar Classification Devices (FNM)
Other Devices by Nu Dimension Tech Ventures LLC
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