gudid
Primary ID: Clarifi
Clarifi Imaging System (UDI Clarifi)
Manufactured by MODULATED IMAGING INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Clarifi Imaging System - Primary ID Clarifi
Device Regulatory Overview
The Clarifi Imaging System (Model/Catalog Number: Clarifi) is a medical device manufactured by MODULATED IMAGING INC.. This product is indexed under FDA Product Code / Category Classification MUD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Clarifi
- Product Code / EMDN
- MUD
- Device Name
- Tissue Saturation Oximeter
- Database Sync Date
- 2026-08-09 09:49:19
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 Clarifi Imaging System?
The registered manufacturer of record for Clarifi Imaging System is MODULATED IMAGING INC..
What is the Primary UDI-DI identifier for Clarifi Imaging System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Clarifi.
What classification code is assigned to this device?
This device is registered under product classification code MUD.
Similar Classification Devices (MUD)
Other Devices by MODULATED IMAGING INC.
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