gudid
Primary ID: 516-850
Solid Vaginal Retractor Frame (UDI 516-850)
Manufactured by SONTEC INSTRUMENTS, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Solid Vaginal Retractor Frame - Primary ID 516-850
Device Regulatory Overview
The Solid Vaginal Retractor Frame (Model/Catalog Number: 516-850) 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
- 516-850
- Product Code / EMDN
- FFO
- Device Name
- Solid Vaginal Retractor Frame Oval 203 Millimeters X 266 Millimeters X 4 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 Solid Vaginal Retractor Frame?
The registered manufacturer of record for Solid Vaginal Retractor Frame is SONTEC INSTRUMENTS, INC..
What is the Primary UDI-DI identifier for Solid Vaginal Retractor Frame?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 516-850.
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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