gudid Primary ID: CMS50DA

Sunbeam (UDI CMS50DA)

Manufactured by Contec Medical Systems Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Sunbeam (Model/Catalog Number: CMS50DA) is a medical device manufactured by Contec Medical Systems Co., Ltd.. This product is indexed under FDA Product Code / Category Classification OCH within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1764-2025 View Full Alert →

CMS8000 Patient Monitor...

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Technical Specifications

Model Number: CMS50DA
Product Code / EMDN: OCH
Device Name: Fingertip Pulse Oximeter
Database Sync Date: 2026-08-09 09:04:20

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 Sunbeam?

The registered manufacturer of record for Sunbeam is Contec Medical Systems Co., Ltd..

What is the Primary UDI-DI identifier for Sunbeam?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CMS50DA.

What classification code is assigned to this device?

This device is registered under product classification code OCH.

Similar Classification Devices (OCH)

Other Devices by Contec Medical Systems Co., Ltd.

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