GUDIDData
eudamed_udi Primary ID: 06950715501009

Compressor Nebulizer (UDI 06950715501009)

Manufactured by Cofoe Medical Technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Compressor Nebulizer - Primary ID 06950715501009

Device Regulatory Overview

The Compressor Nebulizer (Model/Catalog Number: KF-WHQ-07) is a medical device manufactured by Cofoe Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification Z12159002 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KF-WHQ-07
Product Code / EMDN
Z12159002
Device Name
Compressor Nebulizer
Database Sync Date
2026-08-09 16:49:37

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 Compressor Nebulizer?

The registered manufacturer of record for Compressor Nebulizer is Cofoe Medical Technology Co.,Ltd..

What is the Primary UDI-DI identifier for Compressor Nebulizer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06950715501009.

What classification code is assigned to this device?

This device is registered under product classification code Z12159002.

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