gudid
Primary ID: ACC3120
Blazer (UDI ACC3120)
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 ACC3120
Device Regulatory Overview
The Blazer (Model/Catalog Number: ACC3120) is a medical device manufactured by BENVENUE MEDICAL, INC.. This product is indexed under FDA Product Code / Category Classification HTW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ACC3120
- Product Code / EMDN
- HTW
- Device Name
- Blazer Bone Drill
- Database Sync Date
- 2026-08-09 09:43:35
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 ACC3120.
What classification code is assigned to this device?
This device is registered under product classification code HTW.
Similar Classification Devices (HTW)
Other Devices by BENVENUE MEDICAL, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint