"Le Pulse" vein removal device (sterilized) - Taiwan Registration 174c334507b05be1c89f76c4bdacbf03
Access comprehensive regulatory information for "Le Pulse" vein removal device (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 174c334507b05be1c89f76c4bdacbf03 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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Device Details
Product Details
Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
I General, Plastic Surgery and Dermatology
I.4800 Hand Instruments for General Surgery
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Jan 23, 2009
Jan 23, 2024