Taiwan FDA registration befb520ec407132cd7df81eabd9ca30f
Suneside-Yisi endoscope disinfectant
TW: 桑耐賽德-伊思內視鏡消毒液
Registration details
- Analysis ID
- befb520ec407132cd7df81eabd9ca30f
- Customs Code
- DHA05603672101
Company information
- Manufacturer
- THAI AMTEC CO., LTD.;; AMTEC CO., LTD.
- Manufacturer Country
- Thailand;;Japan
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6885 Liquid chemical biocide/highly disinfectant
- Import Information
- import
Dates and status
- Registration Date
- Sep 08, 2023
- Expiry Date
- Sep 08, 2028
About this record
Access comprehensive regulatory information for Suneside-Yisi endoscope disinfectant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number befb520ec407132cd7df81eabd9ca30f and manufactured by THAI AMTEC CO., LTD.;; AMTEC CO., LTD.. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN 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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