eudamed_udi Primary ID: 05707480026371

Ambu® BlueSensor NF (UDI 05707480026371)

Manufactured by Ambu A/S

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ambu® BlueSensor NF (Model/Catalog Number: NF-50-F/12) is a medical device manufactured by Ambu A/S. This product is indexed under FDA Product Code / Category Classification C020501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NF-50-F/12
Product Code / EMDN: C020501
Device Name: BlueSensor Solid gel
Database Sync Date: 2026-08-09 16:28:47

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 Ambu® BlueSensor NF?

The registered manufacturer of record for Ambu® BlueSensor NF is Ambu A/S.

What is the Primary UDI-DI identifier for Ambu® BlueSensor NF?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05707480026371.

What classification code is assigned to this device?

This device is registered under product classification code C020501.

Similar Classification Devices (C020501)

Other Devices by Ambu A/S

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