Taiwan FDA registration 7815ca017ca088dfdeb42612aeac0296
Kesp hydrogen peroxide low-temperature plasma sterilizer
TW: 凱斯普過氧化氫低溫電漿滅菌器
Taiwan·Risk Class 2·MuDanJiang Plasma Physical Application Technology Co., Ltd.·Registered May 25, 2017 – May 25, 2027ActiveRegistration details
- Analysis ID
- 7815ca017ca088dfdeb42612aeac0296
- Customs Code
- DHA09200082709
Company information
- Manufacturer Country
- China
- Authorized Representative
- SMARTECH MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6860 環氧乙烷氣體滅菌器
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- May 25, 2017
- Expiry Date
- May 25, 2027
About this record
Access comprehensive regulatory information for Kesp hydrogen peroxide low-temperature plasma sterilizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7815ca017ca088dfdeb42612aeac0296 and manufactured by MuDanJiang Plasma Physical Application Technology Co., Ltd.. The authorized representative in Taiwan is SMARTECH MEDICAL 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.
Free DatabasePowered by Pure Global AI89,000+ Devices