Taiwan FDA registration bcd39d32e3c8940f3999844a5748d0ec
"Kaiwei" non-powered, single patient use, portable suction device (unsterilized)
TW: “愷威”非動力式，單一病人使用，可攜帶式之抽吸器具（未滅菌）
Taiwan·Risk Class 1·KAIWEI (SHENZHEN) CO., LTD.·Registered Apr 02, 2010 – Apr 02, 2025ExpiredRegistration details
- Analysis ID
- bcd39d32e3c8940f3999844a5748d0ec
- Customs Code
- DHA04600090108
Company information
- Manufacturer
- KAIWEI (SHENZHEN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
Product details
- Intended Use
- Limited to the first level of classification and grading management of medical equipment, "Non-powered, single-patient, portable suction equipment (I.4680)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4680 Non-motive, single patient-use, carry-on suctioning device
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 02, 2010
- Expiry Date
- Apr 02, 2025
About this record
Access comprehensive regulatory information for "Kaiwei" non-powered, single patient use, portable suction device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bcd39d32e3c8940f3999844a5748d0ec and manufactured by KAIWEI (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
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