gudid
Primary ID: ACC1520
Kiva (UDI ACC1520)
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 ACC1520
Device Regulatory Overview
The Kiva (Model/Catalog Number: ACC1520) is a medical device manufactured by BENVENUE MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification GAA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACC1520
- Product Code / EMDN
- GAA
- Device Name
- CorePlus Bone Biopsy Needle, 11GA
- 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 ACC1520.
What classification code is assigned to this device?
This device is registered under product classification code GAA.
Similar Classification Devices (GAA)
Other Devices by BENVENUE MEDICAL, INC.
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