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"Maxtec" Flowmeter (Non-sterile) - Taiwan Registration e1c6a30a47f4fba20b4a7c9f918e762f

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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e1c6a30a47f4fba20b4a7c9f918e762f
Registration Details
Taiwan FDA Registration: e1c6a30a47f4fba20b4a7c9f918e762f
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Device Details

"Maxtec" Flowmeter (Non-sterile)
TW: "้บฅๆ–ฏ็‰นๅ…‹" ้†ซ็™‚็”จๆฐฃ้ซ”ๆต้‡่จˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e1c6a30a47f4fba20b4a7c9f918e762f

Ministry of Health Medical Device Import Registration No. a00128

DHA084a0012800

Company Information

Product Details

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.

D Anesthesiology

D2320 Uncompensated Tube Flow Meter

Dates and Status

Oct 21, 2022

Oct 31, 2023