Taiwan FDA registration 765e7295e03478c1d51b3e67bbf4255a
"Bioden" intravascular catheter fixation device (sterilized/unsterilized)
TW: "百歐登" 血管內導管固定裝置 (滅菌/未滅菌)
Taiwan·Risk Class 1·BIODERM INC.·Registered Mar 01, 2017 – Mar 01, 2022CancelledRegistration details
- Analysis ID
- 765e7295e03478c1d51b3e67bbf4255a
- Customs Code
- DHA09401754201
Company information
- Manufacturer
- BIODERM INC.
- Manufacturer Country
- United States
- Authorized Representative
- HUILI MEDICAL EQUIPMENT LIMITED
Product details
- Intended Use
- Limited to the first level recognition range of endovascular catheter fixation device (J.5210) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5210 血管內導管固定裝置
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 01, 2017
- Expiry Date
- Mar 01, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bioden" intravascular catheter fixation device (sterilized/unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 765e7295e03478c1d51b3e67bbf4255a and manufactured by BIODERM INC.. The authorized representative in Taiwan is HUILI MEDICAL EQUIPMENT LIMITED.
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