gudid
Primary ID: KD205
SnapshotNIR (UDI KD205)
Manufactured by Kent Imaging Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SnapshotNIR - Primary ID KD205
Device Regulatory Overview
The SnapshotNIR (Model/Catalog Number: KD205) is a medical device manufactured by Kent 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
- KD205
- Product Code / EMDN
- MUD
- Device Name
- Tissue oxygenation imaging device
- Database Sync Date
- 2026-08-09 09:18:01
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 SnapshotNIR?
The registered manufacturer of record for SnapshotNIR is Kent Imaging Inc.
What is the Primary UDI-DI identifier for SnapshotNIR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KD205.
What classification code is assigned to this device?
This device is registered under product classification code MUD.
Similar Classification Devices (MUD)
Other Devices by Kent Imaging Inc
Programmatic Export
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JSON API Endpoint