Taiwan FDA registration 626667526b7ad6d225b1ff8e535277a2
"Puwei" laparoscopic gas filter tube (sterilization)
TW: "普威" 腹腔鏡氣體過濾管器 (滅菌)
Taiwan·Risk Class 1·Puwei International Co., Ltd. Yilan Factory·Registered Apr 28, 2017 – Apr 28, 2027ActiveRegistration details
- Analysis ID
- 626667526b7ad6d225b1ff8e535277a2
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 first level identification scope of laparoscopic instillers (L.1730) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.1730 腹腔鏡灌入器
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Apr 28, 2017
- Expiry Date
- Apr 28, 2027
About this record
Access comprehensive regulatory information for "Puwei" laparoscopic gas filter 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 626667526b7ad6d225b1ff8e535277a2 and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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