Pure Global

"Qinda" liquid drug dispenser (unsterilized) - Taiwan Registration 214ed94fbd7d84ca02647bb692c4229f

Access comprehensive regulatory information for "Qinda" liquid drug dispenser (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 214ed94fbd7d84ca02647bb692c4229f and manufactured by HOSPITECH MANUFACTURING SERVICES SDN. BHD.. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT 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
214ed94fbd7d84ca02647bb692c4229f
Registration Details
Taiwan FDA Registration: 214ed94fbd7d84ca02647bb692c4229f
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Qinda" liquid drug dispenser (unsterilized)
TW: โ€œๅ‹ค้”โ€ๆถฒ้ซ”่—ฅ็‰ฉ็ตฆ่—ฅๅ™จ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

214ed94fbd7d84ca02647bb692c4229f

DHA04400679408

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Liquid Drug Dispenser (J.6430)".

J General hospital and personal use equipment

J.6430 ๆถฒ้ซ”่—ฅ็‰ฉ็ตฆ่—ฅๅ™จ

import

Dates and Status

Jun 06, 2008

Jun 06, 2023