Taiwan FDA registration 5a93d1c7211e991406d9ece9ecc30b56
"Pusen" hemodynamic monitoring system and accessories
TW: “普生”血液動力監視系統與配件
Taiwan·Risk Class 2·PULSION MEDICAL SYSTEMS SE·Registered Oct 22, 2010 – Oct 22, 2020CancelledRegistration details
- Analysis ID
- 5a93d1c7211e991406d9ece9ecc30b56
- Customs Code
- DHA00602158900
Company information
- Manufacturer
- PULSION MEDICAL SYSTEMS SE
- Manufacturer Country
- Germany
- Authorized Representative
- CEMMA MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1435 Single-function programmed diagnostic computer
- Import Information
- import
Dates and status
- Registration Date
- Oct 22, 2010
- Expiry Date
- Oct 22, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Pusen" hemodynamic monitoring system and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5a93d1c7211e991406d9ece9ecc30b56 and manufactured by PULSION MEDICAL SYSTEMS SE. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..
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