"Kentley" Kuloti catheter - Taiwan Registration f82cc5250a2077a004be4fdfe97ebec8
Access comprehensive regulatory information for "Kentley" Kuloti catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f82cc5250a2077a004be4fdfe97ebec8 and manufactured by KENDALL- GAMMATRON CO., LTD.. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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
H Gastroenterology and urology
H.5130 ๆณๅฐฟๅฐ็ฎกๅๅ ถ้ไปถ
import
Dates and Status
May 22, 2007
May 22, 2012
Jul 25, 2014
Cancellation Information
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