Pure Global

"Proway" non-powered, single-patient, portable aspiration device (unsterilized) - Taiwan Registration ec7865591a75a33b691125fa0b4c8c04

Access comprehensive regulatory information for "Proway" non-powered, single-patient, portable aspiration device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ec7865591a75a33b691125fa0b4c8c04 and manufactured by Puwei International Co., Ltd. Taishan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..

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
ec7865591a75a33b691125fa0b4c8c04
Registration Details
Taiwan FDA Registration: ec7865591a75a33b691125fa0b4c8c04
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Proway" non-powered, single-patient, portable aspiration device (unsterilized)
TW: "ๆ™ฎๅจ" ้žๅ‹•ๅŠ›ๅผ๏ผŒๅ–ฎไธ€็—…ไบบไฝฟ็”จ๏ผŒๅฏๆ”œๅธถๅผไน‹ๆŠฝๅธๅ™จๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ec7865591a75a33b691125fa0b4c8c04

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of "non-powered, single-patient, portable suction device (I.4680)" under the Measures for the Administration of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4680 Non-motive, single patient-use, carry-on suctioning device

Domestic

Dates and Status

Aug 16, 2011

Aug 16, 2021

Sep 08, 2023

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€