Pure Global

"Teleflex" Medicinal nonventilatorynebulizer (atomizer) (Non-Sterile) - Taiwan Registration 578fd56dcc1f32c0cfbaa02a54dd60c2

Access comprehensive regulatory information for "Teleflex" Medicinal nonventilatorynebulizer (atomizer) (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 578fd56dcc1f32c0cfbaa02a54dd60c2 and manufactured by Hudson Respiratory Care Tecate S.de R.L.de C.V.(A Teleflex Medical Company). The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
578fd56dcc1f32c0cfbaa02a54dd60c2
Registration Details
Taiwan FDA Registration: 578fd56dcc1f32c0cfbaa02a54dd60c2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Teleflex" Medicinal nonventilatorynebulizer (atomizer) (Non-Sterile)
TW: "ๆณฐๅˆฉ็ฆ" ้žๅ‘ผๅธ็”จ้†ซ่—ฅๅ™ด้œงๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

578fd56dcc1f32c0cfbaa02a54dd60c2

Ministry of Health Medical Device Import No. 019116

DHA09401911604

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".

D Devices for anesthesiology

D5640 Non-respiratory medical nebulizer

Imported from abroad

Dates and Status

May 31, 2018

May 31, 2023