Taiwan FDA registration fc8fb99a6d6dcdf9fe9cf2357c6d699f
"Sterry" ethylene oxide (ethylene oxide) sterilizer/aerator
TW: “思泰瑞” 環氧乙烷(氧化乙烯)滅菌鍋/曝氣機
Taiwan·Risk Class 2·STERIS MEXICO, S. DE R. L. DE C.V.·Registered Jul 11, 2013 – Jul 11, 2018CancelledRegistration details
- Analysis ID
- fc8fb99a6d6dcdf9fe9cf2357c6d699f
- Customs Code
- DHA00602460602
Company information
- Manufacturer
- STERIS MEXICO, S. DE R. L. DE C.V.
- Manufacturer Country
- Mexico
- Authorized Representative
- CHUNG TENG MEDICAL INSTRUMENTS 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
- import
Dates and status
- Registration Date
- Jul 11, 2013
- Expiry Date
- Jul 11, 2018
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Sterry" ethylene oxide (ethylene oxide) sterilizer/aerator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc8fb99a6d6dcdf9fe9cf2357c6d699f and manufactured by STERIS MEXICO, S. DE R. L. DE C.V.. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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