Taiwan FDA registration 0922591133d973dcf432d3df79bfa05f
"Bonthe" closed suction tube group (sterilized)
TW: "邦特" 封閉式抽痰管組(滅菌)
Taiwan·Risk Class 1·Bangte Biotechnology Co., Ltd. Yike Factory·Registered Sep 12, 2024 – Sep 12, 2029ActiveRegistration details
- Analysis ID
- 0922591133d973dcf432d3df79bfa05f
Company information
- Manufacturer
- Bangte Biotechnology Co., Ltd. Yike Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOTEQUE CORPORATION
Product details
- Intended Use
- It is limited to the first level identification scope of tracheobronchial suction catheters (D.6810) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Sep 12, 2024
- Expiry Date
- Sep 12, 2029
About this record
Access comprehensive regulatory information for "Bonthe" closed suction tube group (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0922591133d973dcf432d3df79bfa05f and manufactured by Bangte Biotechnology Co., Ltd. Yike Factory. The authorized representative in Taiwan is BIOTEQUE CORPORATION.
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