gudid
Primary ID: 16-0217
Tungsten Carbide Burr (UDI 16-0217)
Manufactured by ELLIQUENCE, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tungsten Carbide Burr - Primary ID 16-0217
Device Regulatory Overview
The Tungsten Carbide Burr (Model/Catalog Number: 16-0217) is a medical device manufactured by ELLIQUENCE, LLC. This product is indexed under FDA Product Code / Category Classification GEY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 16-0217
- Product Code / EMDN
- GEY
- Device Name
- Database Sync Date
- 2026-08-09 09:21:00
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 Tungsten Carbide Burr?
The registered manufacturer of record for Tungsten Carbide Burr is ELLIQUENCE, LLC.
What is the Primary UDI-DI identifier for Tungsten Carbide Burr?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16-0217.
What classification code is assigned to this device?
This device is registered under product classification code GEY.
Similar Classification Devices (GEY)
Other Devices by ELLIQUENCE, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint