gudid
Primary ID: VAK1700
Blazer (UDI VAK1700)
Manufactured by BENVENUE MEDICAL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Blazer - Primary ID VAK1700
Device Regulatory Overview
The Blazer (Model/Catalog Number: VAK1700) is a medical device manufactured by BENVENUE MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification NDN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VAK1700
- Product Code / EMDN
- NDN
- Device Name
- Vertebral Augmentation Cement Kit for Use with Blazer-C
- 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 Blazer?
The registered manufacturer of record for Blazer is BENVENUE MEDICAL, INC..
What is the Primary UDI-DI identifier for Blazer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VAK1700.
What classification code is assigned to this device?
This device is registered under product classification code NDN.
Similar Classification Devices (NDN)
Other Devices by BENVENUE MEDICAL, INC.
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