Taiwan FDA registration 23eb2ee46d1d8b0decf83c78f67fde66
"Nidris" suction tube with sputum collection box (sterilization)
TW: "尼得立斯" 抽痰管附痰液收集盒 (滅菌)
Taiwan·Risk Class 1·ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.·Registered Aug 14, 2017 – Aug 14, 2022CancelledRegistration details
- Analysis ID
- 23eb2ee46d1d8b0decf83c78f67fde66
- Customs Code
- DHA09600317207
Company information
- Manufacturer
- ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- NEEDLELESS 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
- Aug 14, 2017
- Expiry Date
- Aug 14, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nidris" suction tube with sputum collection box (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 23eb2ee46d1d8b0decf83c78f67fde66 and manufactured by ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is NEEDLELESS CORPORATION.
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