Le Ke Mi Catheter Fixation Device (Sterilized) - Taiwan Registration 4557ecee6704a3ff1a7f7b142a4f3979
Access comprehensive regulatory information for Le Ke Mi Catheter Fixation 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 4557ecee6704a3ff1a7f7b142a4f3979 and manufactured by BSN medical GmbH;; BSN MEDICAL GMBH. The authorized representative in Taiwan is GLORIA BIOMED CO., LTD..
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
It is limited to the first level identification scope of the Intravascular Catheter Fixation Device (J.5210) of the Classification and Grading Management Measures for Medical Devices.
J General hospital and personal use equipment
J.5210 ่ก็ฎกๅ งๅฐ็ฎกๅบๅฎ่ฃ็ฝฎ
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Jun 04, 2024
Jun 04, 2029