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"RUHOF" Endozime AW Triple Plus with APA (Non-Sterile) - Taiwan Registration 5bcf4e7d2898c169744322c0a5a9f847

Access comprehensive regulatory information for "RUHOF" Endozime AW Triple Plus with APA (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 5bcf4e7d2898c169744322c0a5a9f847 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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5bcf4e7d2898c169744322c0a5a9f847
Registration Details
Taiwan FDA Registration: 5bcf4e7d2898c169744322c0a5a9f847
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Device Details

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

Registration Details

5bcf4e7d2898c169744322c0a5a9f847

Ministry of Health Medical Device Import No. 016435

DHA09401643505

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 22, 2016

Apr 22, 2026