Taiwan FDA registration e1c6a30a47f4fba20b4a7c9f918e762f
"Maxtec" Flowmeter (Non-sterile)
TW: "麥斯特克" 醫療用氣體流量計 (未滅菌)
Taiwan·Risk Class 1·MD·MAXTEC, LLC·Registered Oct 21, 2022 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- e1c6a30a47f4fba20b4a7c9f918e762f
- License Form
- Ministry of Health Medical Device Import Registration No. a00128
- Customs Code
- DHA084a0012800
Company information
- Manufacturer
- MAXTEC, LLC
- Manufacturer Country
- United States
- Authorized Representative
- FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND)
Product details
- Intended Use
- Limited to the first level identification range of the "Non-compensated Tube Flow Meter (D.2320)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D2320 Uncompensated Tube Flow Meter
Dates and status
- Registration Date
- Oct 21, 2022
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for "Maxtec" Flowmeter (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e1c6a30a47f4fba20b4a7c9f918e762f and manufactured by MAXTEC, LLC. The authorized representative in Taiwan is FISHER & PAYKEL HEALTHCARE ASIA LIMITED, TAIWAN BRANCH (NEW ZEALAND).
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