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"Oka Shin" Madai breathing pipeline (unsterilized) - Taiwan Registration 389aceb827f8f8590f62febaa7c07798

Access comprehensive regulatory information for "Oka Shin" Madai breathing 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 389aceb827f8f8590f62febaa7c07798 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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389aceb827f8f8590f62febaa7c07798
Registration Details
Taiwan FDA Registration: 389aceb827f8f8590f62febaa7c07798
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Device Details

"Oka Shin" Madai breathing pipeline (unsterilized)
TW: โ€œๅฒกๆ–ฐโ€้บป้†‰ๅ‘ผๅธ็ฎก่ทฏ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

389aceb827f8f8590f62febaa7c07798

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the "anesthesia breathing circuit (D.5240)" of the Measures for the Administration of Medical Equipment.

D Anesthesiology

D.5240 ้บป้†‰ๅ‘ผๅธ็ฎก่ทฏ

Domestic

Dates and Status

Aug 10, 2010

Aug 10, 2015

Jun 25, 2018

Cancellation Information

Logged out

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