gudid
Primary ID: 1
Acuity DX+ (UDI 1)
Manufactured by RADMEDIX, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Acuity DX+ - Primary ID 1
Device Regulatory Overview
The Acuity DX+ (Model/Catalog Number: 1) is a medical device manufactured by RADMEDIX, LLC. This product is indexed under FDA Product Code / Category Classification EHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- EHD
- Device Name
- Database Sync Date
- 2026-08-09 09:17:03
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 Acuity DX+?
The registered manufacturer of record for Acuity DX+ is RADMEDIX, LLC.
What is the Primary UDI-DI identifier for Acuity DX+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code EHD.
Similar Classification Devices (EHD)
Other Devices by RADMEDIX, LLC
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