Taiwan FDA registration 8c8141b52e16406d5f4190bbae29393d
“PULSION” PulsioFlex multiparameter monitor
TW: “普生”多功能病患監測系統
Taiwan·Risk Class 2·MD·PULSION MEDICAL SYSTEMS SE·Registered Oct 31, 2016 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 8c8141b52e16406d5f4190bbae29393d
- License Form
- Ministry of Health Medical Device Import No. 028882
- Customs Code
- DHA05602888200
Company information
- Manufacturer
- PULSION MEDICAL SYSTEMS SE
- Manufacturer Country
- Germany
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1435 single-function programmable diagnostic PC
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 31, 2016
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for “PULSION” PulsioFlex multiparameter monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c8141b52e16406d5f4190bbae29393d and manufactured by PULSION MEDICAL SYSTEMS SE. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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