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"Kuken" heat shiki (unsterilized) - Taiwan Registration d6ec891f01b1db608f3e5dc3e85dd829

Access comprehensive regulatory information for "Kuken" heat shiki (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d6ec891f01b1db608f3e5dc3e85dd829 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is JEOU BAO JIANN HEALTH ENTERPRISE 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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d6ec891f01b1db608f3e5dc3e85dd829
Registration Details
Taiwan FDA Registration: d6ec891f01b1db608f3e5dc3e85dd829
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Device Details

"Kuken" heat shiki (unsterilized)
TW: โ€œไน…ไฟๅฅโ€็†ฑๆ•ทๅขŠ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d6ec891f01b1db608f3e5dc3e85dd829

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the "Power Hot Compress Mat (O.5740)" of the Measures for the Classification and Grading of Medical Equipment.

o Physical Medical Sciences

O.5740 ๅ‹•ๅŠ›ๅผ็†ฑๆ•ทๅขŠ

ๅง”่จ—่ฃฝ้€ ;; ๅœ‹็”ข;; QMS/QSD

Dates and Status

Sep 11, 2014

Sep 11, 2024