Flotec (UDI Hose Assembly)

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: Hose Assembly) is a medical device manufactured by FLOTEC INC. This product is indexed under FDA Product Code / Category Classification BYX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Hose Assembly
Product Code / EMDN: BYX
Device Name
Database Sync Date: 2026-08-09 09:06:29

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 Hose Assembly.

What classification code is assigned to this device?

This device is registered under product classification code BYX.

Similar Classification Devices (BYX)

Other Devices by FLOTEC INC

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint