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"Khanma" warm chamber (unsterilized) - Taiwan Registration fa12027813f6d300ca96709abeb6b72c

Access comprehensive regulatory information for "Khanma" warm chamber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa12027813f6d300ca96709abeb6b72c and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is SHIAN JIA MEEI ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SHIAN JIA MEEI ENTERPRISE CO., LTD., and 1 recent registrations in the same category. 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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fa12027813f6d300ca96709abeb6b72c
Registration Details
Taiwan FDA Registration: fa12027813f6d300ca96709abeb6b72c
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Device Details

"Khanma" warm chamber (unsterilized)
TW: "ๆฑ—้ฆฌ" ๆบซ็†ฑ่‰™ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

fa12027813f6d300ca96709abeb6b72c

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

ๅœ‹็”ข;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2026

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