gudid
Primary ID: C07-01038L8
Zethon (UDI C07-01038L8)
Manufactured by ZETHON LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zethon - Primary ID C07-01038L8
Device Regulatory Overview
The Zethon (Model/Catalog Number: C07-01038L8) is a medical device manufactured by ZETHON LIMITED. This product is indexed under FDA Product Code / Category Classification HBE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C07-01038L8
- Product Code / EMDN
- HBE
- Device Name
- BUR - 2.38MM, TWIST DRILL GOLD, 70MM X 1.0MM X 8MM LENGTH
- Database Sync Date
- 2026-08-09 09:08:08
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 Zethon?
The registered manufacturer of record for Zethon is ZETHON LIMITED.
What is the Primary UDI-DI identifier for Zethon?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C07-01038L8.
What classification code is assigned to this device?
This device is registered under product classification code HBE.
Similar Classification Devices (HBE)
Other Devices by ZETHON LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint