gudid
Primary ID: 516-880
Sontec Rectal Blade (UDI 516-880)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sontec Rectal Blade - Primary ID 516-880
Device Regulatory Overview
The Sontec Rectal Blade (Model/Catalog Number: 516-880) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification FFO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 516-880
- Product Code / EMDN
- FFO
- Device Name
- Sontec Rectal Blade 167 Millimeters X 95 Millimeters
- 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 Sontec Rectal Blade?
The registered manufacturer of record for Sontec Rectal Blade is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for Sontec Rectal Blade?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 516-880.
What classification code is assigned to this device?
This device is registered under product classification code FFO.
Similar Classification Devices (FFO)
Other Devices by SONTEC INSTRUMENTS, INC.
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