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"Xinwei" ENT Examination and Treatment Unit (Unsterilized) - Taiwan Registration b275f817e87801756ff7b038cc3282af

Access comprehensive regulatory information for "Xinwei" ENT Examination and Treatment Unit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b275f817e87801756ff7b038cc3282af and manufactured by KUANG HSING BIOTECH CO., LTD.. The authorized representative in Taiwan is SHINWEI INSTRUMENT INDUSTRY 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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b275f817e87801756ff7b038cc3282af
Registration Details
Taiwan FDA Registration: b275f817e87801756ff7b038cc3282af
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Device Details

"Xinwei" ENT Examination and Treatment Unit (Unsterilized)
TW: โ€œๆ–ฐ้Ÿ‹โ€่€ณ้ผปๅ–‰ๆชขๆŸฅๅŠๆฒป็™‚ๆชฏ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b275f817e87801756ff7b038cc3282af

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Examination and Treatment Unit (G.5300)".

G ENT Science

G.5300 ENT examination and treatment table

Domestic;; Contract manufacturing

Dates and Status

May 01, 2012

Mar 15, 2022

Apr 12, 2024

Cancellation Information

Logged out

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