Taiwan FDA registration 021c41b9b705fe782409d09d2b790b55
"Xinfeng" tracheobronchial suction catheter (sterilized)
TW: “新豐”氣管支氣管抽吸導管(滅菌)
Taiwan·Risk Class 1·SYMPHON MEDICAL TECHNOLOGY CO., LTD.·Registered Feb 22, 2008 – Feb 22, 2028ActiveRegistration details
- Analysis ID
- 021c41b9b705fe782409d09d2b790b55
Company information
- Manufacturer
- SYMPHON MEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SYMPHON MEDICAL TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, tracheobronchial suction catheter (D.6810) first level identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Feb 22, 2008
- Expiry Date
- Feb 22, 2028
About this record
Access comprehensive regulatory information for "Xinfeng" tracheobronchial suction catheter (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 021c41b9b705fe782409d09d2b790b55 and manufactured by SYMPHON MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SYMPHON MEDICAL TECHNOLOGY CO., LTD..
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