Taiwan FDA registration 73cfd23be66027665180062fb5e61eb3
Dayan Medical Device Body fluid suction bag (unsterilized)
TW: 大研醫器 體液吸引袋(未滅菌)
Taiwan·Risk Class 1·NK Mechatronics Co., Ltd.;; DAIKEN MEDICAL CO., LTD.·Registered Aug 30, 2022 – Aug 30, 2027ActiveRegistration details
- Analysis ID
- 73cfd23be66027665180062fb5e61eb3
- Customs Code
- DHA09402288601
Company information
- Manufacturer Country
- Thailand;;Japan
- Authorized Representative
- ROTARY TRADING CO., LTD.
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
- QMS/QSD;; 輸入;; 委託製造
Dates and status
- Registration Date
- Aug 30, 2022
- Expiry Date
- Aug 30, 2027
About this record
Access comprehensive regulatory information for Dayan Medical Device Body fluid suction bag (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 73cfd23be66027665180062fb5e61eb3 and manufactured by NK Mechatronics Co., Ltd.;; DAIKEN MEDICAL CO., LTD.. The authorized representative in Taiwan is ROTARY TRADING CO., LTD..
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