Taiwan FDA registration fa57df1c804b125c3c6ce89f981c4e45
"Kaiwei" closed suction sleeve (unsterilized)
TW: “愷威”密閉式抽痰套(未滅菌)
Taiwan·Risk Class 1·KAI WEI (SHENZHEN) CO. LTD.·Registered Nov 29, 2012 – Nov 29, 2022CancelledRegistration details
- Analysis ID
- fa57df1c804b125c3c6ce89f981c4e45
- Customs Code
- DHA04600180109
Company information
- Manufacturer
- KAI WEI (SHENZHEN) CO. LTD.
- Manufacturer Country
- China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
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
Dates and status
- Registration Date
- Nov 29, 2012
- Expiry Date
- Nov 29, 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 "Kaiwei" closed suction sleeve (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number fa57df1c804b125c3c6ce89f981c4e45 and manufactured by KAI WEI (SHENZHEN) CO. LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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