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"Lifetech Corporation" Hertel atrial septal defect occluder - Taiwan Registration 82bc7d5ffe097e89e97a68e8041a2a20

Access comprehensive regulatory information for "Lifetech Corporation" Hertel 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 82bc7d5ffe097e89e97a68e8041a2a20 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.

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82bc7d5ffe097e89e97a68e8041a2a20
Registration Details
Taiwan FDA Registration: 82bc7d5ffe097e89e97a68e8041a2a20
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Device Details

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

Registration Details

82bc7d5ffe097e89e97a68e8041a2a20

DHA09200070100

Company Information

Product Details

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

E Cardiovascular Medicine Science

Chinese goods;; input

Dates and Status

Aug 20, 2015

Aug 20, 2025