gudid Primary ID: DP-M350

CooperSurgical (UDI DP-M350)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CooperSurgical (Model/Catalog Number: DP-M350) is a medical device manufactured by Coopersurgical, Inc.. This product is indexed under FDA Product Code / Category Classification DPW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DP-M350
Product Code / EMDN: DPW
Device Name: Doppler Blood Flow Monitor
Database Sync Date: 2026-08-09 09:19:29

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 CooperSurgical?

The registered manufacturer of record for CooperSurgical is Coopersurgical, Inc..

What is the Primary UDI-DI identifier for CooperSurgical?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DP-M350.

What classification code is assigned to this device?

This device is registered under product classification code DPW.

Similar Classification Devices (DPW)

Other Devices by Coopersurgical, Inc.

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