eudamed_udi Primary ID: 04716770000244

BMFLOW™ (UDI 04716770000244)

Manufactured by Besmed Health Business Corp.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The BMFLOW™ (Model/Catalog Number: CT-19240) is a medical device manufactured by Besmed Health Business Corp.. This product is indexed under FDA Product Code / Category Classification R060201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CT-19240
Product Code / EMDN: R060201
Device Name: BMFLOW™ Generator, Single Heated Circuit Ø10mm
Database Sync Date: 2026-08-09 17:18:28

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 BMFLOW™?

The registered manufacturer of record for BMFLOW™ is Besmed Health Business Corp..

What is the Primary UDI-DI identifier for BMFLOW™?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04716770000244.

What classification code is assigned to this device?

This device is registered under product classification code R060201.

Similar Classification Devices (R060201)

Other Devices by Besmed Health Business Corp.

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