gudid
Primary ID: RT-4536-NS50
Pronumbra (UDI RT-4536-NS50)
Manufactured by MEDTEC, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pronumbra - Primary ID RT-4536-NS50
Device Regulatory Overview
The Pronumbra (Model/Catalog Number: RT-4536-NS50) is a medical device manufactured by MEDTEC, INC.. This product is indexed under FDA Product Code / Category Classification IXQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RT-4536-NS50
- Product Code / EMDN
- IXQ
- Device Name
- Pronumbra Neck Support, 50mm
- Database Sync Date
- 2026-08-09 09:39:26
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 Pronumbra?
The registered manufacturer of record for Pronumbra is MEDTEC, INC..
What is the Primary UDI-DI identifier for Pronumbra?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RT-4536-NS50.
What classification code is assigned to this device?
This device is registered under product classification code IXQ.
Similar Classification Devices (IXQ)
Other Devices by MEDTEC, INC.
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