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"Lifetech Corporation" Xiruixin atrial septal defect occluder - Taiwan Registration bae46ad396c0a1569777c925f28470a7

Access comprehensive regulatory information for "Lifetech Corporation" Xiruixin atrial septal defect occluder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bae46ad396c0a1569777c925f28470a7 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.

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bae46ad396c0a1569777c925f28470a7
Registration Details
Taiwan FDA Registration: bae46ad396c0a1569777c925f28470a7
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Device Details

"Lifetech Corporation" Xiruixin atrial septal defect occluder
TW: โ€œๅ…ˆๅฅ็ง‘ๆŠ€ๅ…ฌๅธโ€ๅธŒ็‘žๅฟƒๆˆฟ้–“้š”็ผบๆๅฐๅ ตๅ™จ
Risk Class 3

Registration Details

bae46ad396c0a1569777c925f28470a7

DHA09200101106

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.9999 Miscellaneous

The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". Input;; Chinese goods

Dates and Status

Apr 25, 2019

Apr 25, 2029