"Merotek" Nevix movable catheter - Taiwan Registration 4280899ce480a7e50d1f39f7c6ae291b
Access comprehensive regulatory information for "Merotek" Nevix movable catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4280899ce480a7e50d1f39f7c6ae291b and manufactured by MYELOTEC, INC.. The authorized representative in Taiwan is REVO LASER CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
D Anesthesiology
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import
Dates and Status
Jul 27, 2012
Jul 27, 2022
Apr 12, 2024
Cancellation Information
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