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"RUHOF" Endozime Xtreme Power (Non-Sterile) - Taiwan Registration c354f427fc472cb3a0b5fcc3fa43cdd2

Access comprehensive regulatory information for "RUHOF" Endozime Xtreme Power (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c354f427fc472cb3a0b5fcc3fa43cdd2 and manufactured by THE RUHOF CORPORATION. The authorized representative in Taiwan is HONYOU DEVELOPMENT 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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c354f427fc472cb3a0b5fcc3fa43cdd2
Registration Details
Taiwan FDA Registration: c354f427fc472cb3a0b5fcc3fa43cdd2
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Device Details

"RUHOF" Endozime Xtreme Power (Non-Sterile)
TW: "็พ…็ฆ" ้†ซ็™‚ๅ™จๆขฐๅคš้…ถๆธ…ๆด—ๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c354f427fc472cb3a0b5fcc3fa43cdd2

Ministry of Health Medical Device Import No. 016466

DHA09401646603

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".

J General hospital and personal use equipment

J6890 Disinfectants for general medical devices

Imported from abroad

Dates and Status

Apr 28, 2016

Apr 28, 2026