gudid
Primary ID: 355-219
Plate Cutter (UDI 355-219)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Plate Cutter - Primary ID 355-219
Device Regulatory Overview
The Plate Cutter (Model/Catalog Number: 355-219) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification FZT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 355-219
- Product Code / EMDN
- FZT
- Device Name
- Plate Cutter For Titanium Plates (Cuts Up To 1.8 Millimeter Max)
- Database Sync Date
- 2026-08-09 09:07:00
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 Plate Cutter?
The registered manufacturer of record for Plate Cutter is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for Plate Cutter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 355-219.
What classification code is assigned to this device?
This device is registered under product classification code FZT.
Similar Classification Devices (FZT)
Other Devices by SONTEC INSTRUMENTS, INC.
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