Taiwan FDA registration c9a0afccd0714b85fae597eef970f174
“STERIS” Verify V24I SELF-CONTAINED Biological Monitoring
TW: “思泰瑞”低溫滅菌生物監測組
Taiwan·Risk Class 2·MD·STERIS Corporation·Registered Mar 17, 2016 – Mar 17, 2026ExpiredRegistration details
- Analysis ID
- c9a0afccd0714b85fae597eef970f174
- License Form
- Ministry of Health Medical Device Import No. 028332
- Customs Code
- DHA05602833204
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)
- J2800 Sterilization Process Indicator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 17, 2016
- Expiry Date
- Mar 17, 2026
About this record
Access comprehensive regulatory information for “STERIS” Verify V24I SELF-CONTAINED Biological Monitoring in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c9a0afccd0714b85fae597eef970f174 and manufactured by STERIS Corporation. The authorized representative in Taiwan is CHUNG TENG MEDICAL INSTRUMENTS CO., LTD..
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