O2-Sensor (UDI MLF-16DE)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The O2-Sensor (Model/Catalog Number: MLF-16DE) is a medical device manufactured by IT Dr. Gambert GmbH. This product is indexed under FDA Product Code / Category Classification CCL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MLF-16DE
Product Code / EMDN: CCL
Device Name
Database Sync Date: 2026-08-09 09:11:40

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 O2-Sensor?

The registered manufacturer of record for O2-Sensor is IT Dr. Gambert GmbH.

What is the Primary UDI-DI identifier for O2-Sensor?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MLF-16DE.

What classification code is assigned to this device?

This device is registered under product classification code CCL.

Similar Classification Devices (CCL)

Other Devices by IT Dr. Gambert GmbH

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