gudid
Primary ID: KMI-111
Swabeze (UDI KMI-111)
Manufactured by KENTEC MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Swabeze - Primary ID KMI-111
Device Regulatory Overview
The Swabeze (Model/Catalog Number: KMI-111) is a medical device manufactured by KENTEC MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification KXF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KMI-111
- Product Code / EMDN
- KXF
- Device Name
- foam swab
- Database Sync Date
- 2026-08-09 09:33:03
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 Swabeze?
The registered manufacturer of record for Swabeze is KENTEC MEDICAL, INC..
What is the Primary UDI-DI identifier for Swabeze?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KMI-111.
What classification code is assigned to this device?
This device is registered under product classification code KXF.
Similar Classification Devices (KXF)
Other Devices by KENTEC MEDICAL, INC.
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