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"Shinto" vacuum drawing bottle - Taiwan Registration 5f940bade6eb72541416e3f648545ac8

Access comprehensive regulatory information for "Shinto" vacuum drawing bottle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f940bade6eb72541416e3f648545ac8 and manufactured by TAIWAN BIOTECH CO., LTD.. The authorized representative in Taiwan is TAIWAN BIOTECH 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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5f940bade6eb72541416e3f648545ac8
Registration Details
Taiwan FDA Registration: 5f940bade6eb72541416e3f648545ac8
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Device Details

"Shinto" vacuum drawing bottle
TW: โ€œไฟกๆฑโ€็œŸ็ฉบๅผ•ๆต็“ถ
Risk Class 1
Cancelled

Registration Details

5f940bade6eb72541416e3f648545ac8

Company Information

Taiwan, Province of China

Product Details

It is limited to the first level of identification scope of the Administrative Measures for Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".

J General hospital and personal use equipment

J.6740 Vacuum-powered fluid absorption apparatus

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jul 14, 2006

Jul 14, 2016

Aug 09, 2018

Cancellation Information

Logged out

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