eudamed_udi Primary ID: D-CA-63700P7

BMFLOW™ Generator (UDI D-CA-63700P7)

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™ Generator (Model/Catalog Number: CA-63700) is a medical device manufactured by Besmed Health Business Corp.. This product is indexed under FDA Product Code / Category Classification R02010402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CA-63700
Product Code / EMDN: R02010402
Device Name: BMFLOW™ Generator
Database Sync Date: 2026-08-09 18:10:05

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™ Generator?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-CA-63700P7.

What classification code is assigned to this device?

This device is registered under product classification code R02010402.

Similar Classification Devices (R02010402)

Other Devices by Besmed Health Business Corp.

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