Taiwan FDA registration 2e00feef62dada523be424b57878f9b7
"Atrien" marine autologous blood retrieval chest drainage blood reservoir
TW: “亞翠恩”海洋自體血液回收胸腔引流儲血器
Taiwan·Risk Class 2·Atrium Medical Corporation·Registered Mar 23, 2009 – Mar 23, 2024ExpiredRegistration details
- Analysis ID
- 2e00feef62dada523be424b57878f9b7
- Customs Code
- DHA00601972901
Company information
- Manufacturer
- Atrium Medical Corporation
- Manufacturer Country
- United States
- 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)
- J General hospital and personal use equipment;; D Anesthesiology Science
- Product Type (Level 2)
- D.5830 Instruments for automatic blood transfer; J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- import
Dates and status
- Registration Date
- Mar 23, 2009
- Expiry Date
- Mar 23, 2024
About this record
Access comprehensive regulatory information for "Atrien" marine autologous blood retrieval chest drainage blood reservoir in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2e00feef62dada523be424b57878f9b7 and manufactured by Atrium Medical Corporation. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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