NA (UDI CS 750)

Manufactured by Belimed AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The NA (Model/Catalog Number: CS 750) is a medical device manufactured by Belimed AG. This product is indexed under FDA Product Code / Category Classification FLH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CS 750
Product Code / EMDN: FLH
Device Name
Database Sync Date: 2026-08-09 09:16:13

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 NA?

The registered manufacturer of record for NA is Belimed AG.

What is the Primary UDI-DI identifier for NA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CS 750.

What classification code is assigned to this device?

This device is registered under product classification code FLH.

Similar Classification Devices (FLH)

Other Devices by Belimed AG

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