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“RUHOF” Prepzyme Forever Wet (Non-Sterile) - Taiwan Registration ff9e070b9a260b90dffc0b0dec7b2dc0

Access comprehensive regulatory information for “RUHOF” Prepzyme Forever Wet (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 ff9e070b9a260b90dffc0b0dec7b2dc0 and manufactured by THE RUHOF CORPORATION. The authorized representative in Taiwan is HONYOU DEVELOPMENT CO., LTD..

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ff9e070b9a260b90dffc0b0dec7b2dc0
Registration Details
Taiwan FDA Registration: ff9e070b9a260b90dffc0b0dec7b2dc0
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Device Details

“RUHOF” Prepzyme Forever Wet (Non-Sterile)
TW: “羅福” 器械運輸保濕預清洗劑 (未滅菌)
Risk Class 1
MD

Registration Details

ff9e070b9a260b90dffc0b0dec7b2dc0

Ministry of Health Medical Device Import No. 019505

DHA09401950502

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

Aug 16, 2018

Aug 16, 2028