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"Le Pulse" Putt vascular occlusion catheter - Taiwan Registration 30daebc2f0f4880ece3eee61c4b554a7

Access comprehensive regulatory information for "Le Pulse" Putt vascular occlusion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 30daebc2f0f4880ece3eee61c4b554a7 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..

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30daebc2f0f4880ece3eee61c4b554a7
Registration Details
Taiwan FDA Registration: 30daebc2f0f4880ece3eee61c4b554a7
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Device Details

"Le Pulse" Putt vascular occlusion catheter
TW: โ€œๆจ‚่„ˆโ€ๆ™ฎ็‰น่ก€็ฎก้–‰ๅกžๅฐŽ็ฎก
Risk Class 2

Registration Details

30daebc2f0f4880ece3eee61c4b554a7

DHA00601930701

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.1240 ๆต้‡ๅฐŽๅ‘ๅฐŽ็ฎก

import

Dates and Status

Oct 28, 2008

Oct 28, 2028