Taiwan FDA registration 6a52ea31fa6c2d2fbd2a75d9af07855b
"Pusen" Severus central vein oxygen saturation monitoring system and accessories
TW: “普生”西弗斯中央靜脈血氧飽和度監視系統與配件
Taiwan·Risk Class 2·PULSION MEDICAL SYSTEMS SE·Registered Jan 23, 2009 – Jan 23, 2024ExpiredRegistration details
- Analysis ID
- 6a52ea31fa6c2d2fbd2a75d9af07855b
- Customs Code
- DHA00601958309
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 Medicine Science
- Product Type (Level 2)
- E.1435 Single-function programmed diagnostic computer
- Import Information
- import
Dates and status
- Registration Date
- Jan 23, 2009
- Expiry Date
- Jan 23, 2024
About this record
Access comprehensive regulatory information for "Pusen" Severus central vein oxygen saturation 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 6a52ea31fa6c2d2fbd2a75d9af07855b and manufactured by PULSION MEDICAL SYSTEMS SE. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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