"Le Pulse" non-balloon occlusive catheter - Taiwan Registration 1a9e6dd79452f034c451c4fcc37ef9ee
Access comprehensive regulatory information for "Le Pulse" non-balloon occlusive catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a9e6dd79452f034c451c4fcc37ef9ee 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
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.1250 Percutaneous catheters
import
Dates and Status
Nov 20, 2012
Nov 20, 2017
Dec 20, 2019
Cancellation Information
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