gudid
Primary ID: FGS-9000-19
Versaflex (UDI FGS-9000-19)
Manufactured by Given Imaging, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Versaflex - Primary ID FGS-9000-19
Device Regulatory Overview
The Versaflex (Model/Catalog Number: FGS-9000-19) is a medical device manufactured by Given Imaging, Inc.. This product is indexed under FDA Product Code / Category Classification FFT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FGS-9000-19
- Product Code / EMDN
- FFT
- Device Name
- Disposable pH / Impedance Catheter, Dual pH Sensor, 22cm, 8 Impedance Rings, LPR ZNID22+8R
- Database Sync Date
- 2026-08-09 09:17:35
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 Versaflex?
The registered manufacturer of record for Versaflex is Given Imaging, Inc..
What is the Primary UDI-DI identifier for Versaflex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FGS-9000-19.
What classification code is assigned to this device?
This device is registered under product classification code FFT.
Similar Classification Devices (FFT)
Other Devices by Given Imaging, Inc.
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