O2-Sensor (UDI MLF-16H)

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-16H) 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-16H
Product Code / EMDN: CCL
Device Name
Database Sync Date: 2026-08-09 09:11:40

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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-16H.

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint