gudid
Primary ID: 508-556
O-RING HEMORRHOID BAND CUTTER (UDI 508-556)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for O-RING HEMORRHOID BAND CUTTER - Primary ID 508-556
Device Regulatory Overview
The O-RING HEMORRHOID BAND CUTTER (Model/Catalog Number: 508-556) 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
- 508-556
- Product Code / EMDN
- FZT
- Device Name
- O-RING HEMORRHOID BAND CUTTER
- Database Sync Date
- 2026-08-09 09:07:04
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 O-RING HEMORRHOID BAND CUTTER?
The registered manufacturer of record for O-RING HEMORRHOID BAND CUTTER is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for O-RING HEMORRHOID BAND CUTTER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 508-556.
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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