gudid Primary ID: PC-60FW

Pulse Oximeter (UDI PC-60FW)

Manufactured by Shenzhen Creative Industry Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Pulse Oximeter (Model/Catalog Number: PC-60FW) is a medical device manufactured by Shenzhen Creative Industry Co., Ltd.. This product is indexed under FDA Product Code / Category Classification DQA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PC-60FW
Product Code / EMDN: DQA
Device Name
Database Sync Date: 2026-08-09 09:04:48

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 Pulse Oximeter?

The registered manufacturer of record for Pulse Oximeter is Shenzhen Creative Industry Co., Ltd..

What is the Primary UDI-DI identifier for Pulse Oximeter?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PC-60FW.

What classification code is assigned to this device?

This device is registered under product classification code DQA.

Similar Classification Devices (DQA)

Other Devices by Shenzhen Creative Industry Co., Ltd.

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