gudid
Primary ID: 16-0204
Surgi-Max Drill (UDI 16-0204)
Manufactured by ELLIQUENCE, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Surgi-Max Drill - Primary ID 16-0204
Device Regulatory Overview
The Surgi-Max Drill (Model/Catalog Number: 16-0204) 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
- 16-0204
- Product Code / EMDN
- GEY
- Device Name
- Diamond Spinal Burr, One (1) Sterile, Single Use, Dia:5.0mm, WL:185mm
- 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
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Surgi-Max Drill?
The registered manufacturer of record for Surgi-Max Drill is ELLIQUENCE, LLC.
What is the Primary UDI-DI identifier for Surgi-Max Drill?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16-0204.
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
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