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“Foremount” Nebulizer Kit and Accessory (Non-Sterile) - Taiwan Registration 419ae7c7f80931ed7986b787f9cb7479

Access comprehensive regulatory information for “Foremount” Nebulizer Kit and Accessory (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 419ae7c7f80931ed7986b787f9cb7479 and manufactured by HEADSTAR MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is FOREMOUNT ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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419ae7c7f80931ed7986b787f9cb7479
Registration Details
Taiwan FDA Registration: 419ae7c7f80931ed7986b787f9cb7479
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Device Details

“Foremount” Nebulizer Kit and Accessory (Non-Sterile)
TW: “遠貿”噴霧罐組及配件(未滅菌)
Risk Class 2
MD

Registration Details

419ae7c7f80931ed7986b787f9cb7479

Ministry of Health Medical Device Manufacturing No. 006439

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5630 Sprayer

Produced in Taiwan, China; Contract manufacturing

Dates and Status

Jul 02, 2019

Jul 02, 2024