Taiwan FDA registration 01812c6ce4b7a2c44d8a5412fae144cd
"Sterix" biosterilization indicator group
TW: “思泰瑞”生物滅菌指示劑組
Taiwan·Risk Class 2·STERIS Corporation·Registered Aug 28, 2012 – Aug 28, 2027ActiveRegistration details
- Analysis ID
- 01812c6ce4b7a2c44d8a5412fae144cd
- Customs Code
- DHA00602394302
Company information
- Manufacturer
- STERIS Corporation
- Manufacturer Country
- United States
- 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.2800 Sterilization Process Indicator
- Import Information
- import
Dates and status
- Registration Date
- Aug 28, 2012
- Expiry Date
- Aug 28, 2027
About this record
Access comprehensive regulatory information for "Sterix" biosterilization indicator group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01812c6ce4b7a2c44d8a5412fae144cd and manufactured by STERIS Corporation. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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