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"Oka Shin" respiratory pipeline (unsterilized) - Taiwan Registration 1fbadc421d5fc237e54d385f90cd1c6a

Access comprehensive regulatory information for "Oka Shin" respiratory pipeline (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1fbadc421d5fc237e54d385f90cd1c6a and manufactured by KUNG SHIN PLASTICS CO., LTD.. The authorized representative in Taiwan is KUNG SHIN PLASTICS CO., 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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1fbadc421d5fc237e54d385f90cd1c6a
Registration Details
Taiwan FDA Registration: 1fbadc421d5fc237e54d385f90cd1c6a
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Device Details

"Oka Shin" respiratory pipeline (unsterilized)
TW: โ€œๅฒกๆ–ฐโ€ๅ‘ผๅธๅ™จ็ฎก่ทฏ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

1fbadc421d5fc237e54d385f90cd1c6a

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "Respirator Tubing (D.5975)" of the Measures for the Administration of Medical Equipment.

D Anesthesiology

D.5975 Respirator Tubing

Domestic

Dates and Status

Aug 10, 2010

Aug 10, 2015

Jun 25, 2018

Cancellation Information

Logged out

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