Flotec (UDI RW Regulator)

Manufactured by FLOTEC INC

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Flotec (Model/Catalog Number: RW Regulator) is a medical device manufactured by FLOTEC INC. This product is indexed under FDA Product Code / Category Classification CAN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: RW Regulator
Product Code / EMDN: CAN
Device Name
Database Sync Date: 2026-08-09 09:06:29

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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Frequently Asked Questions

Who is the primary manufacturer of Flotec?

The registered manufacturer of record for Flotec is FLOTEC INC.

What is the Primary UDI-DI identifier for Flotec?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is RW Regulator.

What classification code is assigned to this device?

This device is registered under product classification code CAN.

Similar Classification Devices (CAN)

Other Devices by FLOTEC INC

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