gudid
Primary ID: FX10
Flo-X (UDI FX10)
Manufactured by MINIMALLY INVASIVE DEVICES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Flo-X - Primary ID FX10
Device Regulatory Overview
The Flo-X (Model/Catalog Number: FX10) is a medical device manufactured by MINIMALLY INVASIVE DEVICES, INC.. This product is indexed under FDA Product Code / Category Classification OCT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FX10
- Product Code / EMDN
- OCT
- Device Name
- The Defogging and Cleaning Solution is a single-use laparoscopic accessory device intended to facilitate intra-operative defogging and cleaning of the lens of a laparoscope during minimally invasive surgery while maintaining visualization of the surgical site.
- Database Sync Date
- 2026-08-09 09:40:21
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 Flo-X?
The registered manufacturer of record for Flo-X is MINIMALLY INVASIVE DEVICES, INC..
What is the Primary UDI-DI identifier for Flo-X?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is FX10.
What classification code is assigned to this device?
This device is registered under product classification code OCT.
Similar Classification Devices (OCT)
Other Devices by MINIMALLY INVASIVE DEVICES, INC.
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