Taiwan FDA registration 9246598df4fd1da9ae990493c4d685a1
"Aon" sputum collection box with sputum suction tube (sterilization)
TW: 〝怡安〞抽痰管附痰液收集盒 (滅菌)
Taiwan·Risk Class 1·ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.·Registered Dec 21, 2011 – Dec 21, 2021CancelledRegistration details
- Analysis ID
- 9246598df4fd1da9ae990493c4d685a1
- Customs Code
- DHA04600154708
Company information
- Manufacturer
- ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- LILY MEDICAL CORPORATION
Product details
- Intended Use
- Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- Chinese goods;; Input;; QMS/QSD
Dates and status
- Registration Date
- Dec 21, 2011
- Expiry Date
- Dec 21, 2021
- Cancellation Date
- Sep 19, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Aon" sputum collection box with sputum suction tube (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9246598df4fd1da9ae990493c4d685a1 and manufactured by ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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