gudid
Primary ID: RMXS5000
DYNATRONICS (UDI RMXS5000)
Manufactured by ARMEDICA MANUFACTURING CORP.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DYNATRONICS - Primary ID RMXS5000
Device Regulatory Overview
The DYNATRONICS (Model/Catalog Number: RMXS5000) is a medical device manufactured by ARMEDICA MANUFACTURING CORP.. This product is indexed under FDA Product Code / Category Classification INQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- RMXS5000
- Product Code / EMDN
- INQ
- Device Name
- STEEL, ELECTRIC, X FRAME, THREE SECTION, 27 IN WIDE TREATMENT TABLE WITH ADJUSTABLE HEAD SECTION, ADJUSTABLE ARMRESTS, ADJUSTABLE FOOT SECTION, AND CASTERS
- Database Sync Date
- 2026-08-09 09:06:23
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 DYNATRONICS?
The registered manufacturer of record for DYNATRONICS is ARMEDICA MANUFACTURING CORP..
What is the Primary UDI-DI identifier for DYNATRONICS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RMXS5000.
What classification code is assigned to this device?
This device is registered under product classification code INQ.
Similar Classification Devices (INQ)
Other Devices by ARMEDICA MANUFACTURING CORP.
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