"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
Device Details
"Lifetech Corporation" Hertel atrial septal defect occluder
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Risk Class 3

