gudid
Primary ID: 1
Radmedix AcuityDRe 1717t (UDI 1)
Manufactured by RADMEDIX, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Radmedix AcuityDRe 1717t - Primary ID 1
Device Regulatory Overview
The Radmedix AcuityDRe 1717t (Model/Catalog Number: 1) is a medical device manufactured by RADMEDIX, LLC. This product is indexed under FDA Product Code / Category Classification MQB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- MQB
- 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 Radmedix AcuityDRe 1717t?
The registered manufacturer of record for Radmedix AcuityDRe 1717t is RADMEDIX, LLC.
What is the Primary UDI-DI identifier for Radmedix AcuityDRe 1717t?
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 MQB.
Similar Classification Devices (MQB)
Other Devices by RADMEDIX, LLC
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