Taiwan FDA registration 5bcf4e7d2898c169744322c0a5a9f847

"RUHOF" Endozime AW Triple Plus with APA (Non-Sterile)

TW: "羅福" 醫療器械多酶清洗劑 (未滅菌)

Taiwan·Risk Class 1·MD·THE RUHOF CORPORATION·Registered Apr 22, 2016 – Apr 22, 2026Expired

Registration details

Analysis ID: 5bcf4e7d2898c169744322c0a5a9f847
License Form: Ministry of Health Medical Device Import No. 016435
Customs Code: DHA09401643505

Company information

Manufacturer: THE RUHOF CORPORATION
Manufacturer Country: United States
Authorized Representative: HONYOU DEVELOPMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Disinfectants for General Medical Devices (J.6890)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J6890 Disinfectants for general medical devices
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 22, 2016
Expiry Date: Apr 22, 2026

About this record

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..

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