gudid
Primary ID: KIV2250
Kiva (UDI KIV2250)
Manufactured by BENVENUE MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kiva - Primary ID KIV2250
Device Regulatory Overview
The Kiva (Model/Catalog Number: KIV2250) is a medical device manufactured by BENVENUE MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification LOD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KIV2250
- Product Code / EMDN
- LOD
- Device Name
- Kiva VCF Treatment System, Additional Fracture Kit, Left
- Database Sync Date
- 2026-08-09 09:43:35
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 Kiva?
The registered manufacturer of record for Kiva is BENVENUE MEDICAL, INC..
What is the Primary UDI-DI identifier for Kiva?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KIV2250.
What classification code is assigned to this device?
This device is registered under product classification code LOD.
Similar Classification Devices (LOD)
Other Devices by BENVENUE MEDICAL, INC.
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