Pure Global

"Qinda" non-respiratory medical sprayer (unsterilized) - Taiwan Registration 18344d3737be3268e9f1201dd661dd0b

Access comprehensive regulatory information for "Qinda" non-respiratory medical sprayer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18344d3737be3268e9f1201dd661dd0b 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
18344d3737be3268e9f1201dd661dd0b
Registration Details
Taiwan FDA Registration: 18344d3737be3268e9f1201dd661dd0b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Qinda" non-respiratory medical sprayer (unsterilized)
TW: โ€œๅ‹ค้”โ€้žๅ‘ผๅธ็”จ้†ซ่—ฅๅ™ด้œงๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

18344d3737be3268e9f1201dd661dd0b

DHA04401160206

Company Information

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 Anesthesiology

D.5640 ้žๅ‘ผๅธ็”จ้†ซ่—ฅๅ™ด้œงๅ™จ(atomizer)

import

Dates and Status

Apr 16, 2012

Apr 16, 2022

Apr 12, 2024

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ