Taiwan FDA registration f4dedcf0cdef738ebf7a7681a94b6099
"Michael Air" non-powered, single-patient, portable suction device (unsterilized)
TW: "麥可艾爾" 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·MicroAire Surgical Instruments, LLC·Registered Sep 05, 2011 – Sep 05, 2026ActiveRegistration details
- Analysis ID
- f4dedcf0cdef738ebf7a7681a94b6099
- Customs Code
- DHA04401080107
Company information
- Manufacturer
- MicroAire Surgical Instruments, LLC
- Manufacturer Country
- United States
- Authorized Representative
- ACL BIOMEDICAL 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
- import
Dates and status
- Registration Date
- Sep 05, 2011
- Expiry Date
- Sep 05, 2026
About this record
Access comprehensive regulatory information for "Michael Air" non-powered, single-patient, 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 f4dedcf0cdef738ebf7a7681a94b6099 and manufactured by MicroAire Surgical Instruments, LLC. The authorized representative in Taiwan is ACL BIOMEDICAL CO., LTD..
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