gudid
Primary ID: 017381
Accessory Kit (UDI 017381)
Manufactured by Bracco Injeneering SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Accessory Kit - Primary ID 017381
Device Regulatory Overview
The Accessory Kit (Model/Catalog Number: 017381) is a medical device manufactured by Bracco Injeneering SA. This product is indexed under FDA Product Code / Category Classification IZQ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 017381
- Product Code / EMDN
- IZQ
- Device Name
- Database Sync Date
- 2026-08-09 09:59:20
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 Accessory Kit?
The registered manufacturer of record for Accessory Kit is Bracco Injeneering SA.
What is the Primary UDI-DI identifier for Accessory Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 017381.
What classification code is assigned to this device?
This device is registered under product classification code IZQ.
Similar Classification Devices (IZQ)
Other Devices by Bracco Injeneering SA
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint