Taiwan FDA registration a03b7be526691d35a1c8ee620b6801c7
"Prowei" closed suction sleeve (sterilized)
TW: “普威”密閉式抽痰套 (滅菌)
Taiwan·Risk Class 1·Puwei International Co., Ltd. Yilan Factory·Registered Jun 22, 2010 – Jun 22, 2025ExpiredRegistration details
- Analysis ID
- a03b7be526691d35a1c8ee620b6801c7
Company information
- Manufacturer
- Puwei International Co., Ltd. Yilan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
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
- Jun 22, 2010
- Expiry Date
- Jun 22, 2025
About this record
Access comprehensive regulatory information for "Prowei" closed suction sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a03b7be526691d35a1c8ee620b6801c7 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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