gudid
Primary ID: C07-01038L4
Zethon (UDI C07-01038L4)
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 C07-01038L4
Device Regulatory Overview
The Zethon (Model/Catalog Number: C07-01038L4) 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
- C07-01038L4
- Product Code / EMDN
- HBE
- Device Name
- BUR - 2.38MM, TWIST DRILL GOLD, 70MM X 1.0MM X 4MM LENGTH
- Database Sync Date
- 2026-08-09 09:08:08
Full Regulatory Attributes
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{
"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 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 C07-01038L4.
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
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