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"Pacific" extraction apparatus (sterile) - Taiwan Registration 55f6b6cdbe441dff06d05fa66ad46c90

Access comprehensive regulatory information for "Pacific" extraction apparatus (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 55f6b6cdbe441dff06d05fa66ad46c90 and manufactured by Pacific Medical Materials Co., Ltd. Copper Factory. The authorized representative in Taiwan is PACIFIC HOSPITAL SUPPLY 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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55f6b6cdbe441dff06d05fa66ad46c90
Registration Details
Taiwan FDA Registration: 55f6b6cdbe441dff06d05fa66ad46c90
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Device Details

"Pacific" extraction apparatus (sterile)
TW: โ€œๅคชๅนณๆด‹โ€ๆŠฝๅธๅ™จๅ…ท (ๆป…่Œ)
Risk Class 1

Registration Details

55f6b6cdbe441dff06d05fa66ad46c90

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the classification and grading management measures for medical equipment "Vacuum-powered body fluid absorption device (J.6740)".

J General hospital and personal use equipment

J.6740 Vacuum-powered fluid absorption apparatus

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Mar 07, 2014

Mar 07, 2029