Taiwan FDA registration 1dc12ce3bf2b6a53b7709b1d8c723ddb
“Finetech” Transducer Protector (Sterile)
TW: “釩泰”壓力監測器保護罩(已滅菌)
Taiwan·Risk Class 2·MD·FINETECH RESEARCH AND INNOVATION CORPORATION·Registered Feb 17, 2017 – Feb 17, 2022CancelledRegistration details
- Analysis ID
- 1dc12ce3bf2b6a53b7709b1d8c723ddb
- License Form
- Ministry of Health Medical Device Manufacturing No. 005703
Company information
- Manufacturer
- FINETECH RESEARCH AND INNOVATION CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FINETECH RESEARCH AND INNOVATION CORPORATION
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5820 Hemodialysis systems and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Feb 17, 2017
- Expiry Date
- Feb 17, 2022
- Cancellation Date
- Oct 05, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Finetech” Transducer Protector (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1dc12ce3bf2b6a53b7709b1d8c723ddb and manufactured by FINETECH RESEARCH AND INNOVATION CORPORATION. The authorized representative in Taiwan is FINETECH RESEARCH AND INNOVATION CORPORATION.
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