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"Lifetech Technology Company" Shri elastic interatrial septal occluder - Taiwan Registration f0099f666cb296dd282b3083a031a0c3

Access comprehensive regulatory information for "Lifetech Technology Company" Shri elastic interatrial septal occluder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f0099f666cb296dd282b3083a031a0c3 and manufactured by LifeTech Scientific (Europe) Coรถperatief U.A.. The authorized representative in Taiwan is KAISEN MEDICAL CO., LTD.

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f0099f666cb296dd282b3083a031a0c3
Registration Details
Taiwan FDA Registration: f0099f666cb296dd282b3083a031a0c3
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Device Details

"Lifetech Technology Company" Shri elastic interatrial septal occluder
TW: โ€œๅ…ˆๅฅ็ง‘ๆŠ€ๅ…ฌๅธโ€ ๅธŒ็‘žๅฝˆๆ€งๅฟƒๆˆฟ้–“้š”็ผบๆๅฐๅ ตๅ™จ
Risk Class 3

Registration Details

f0099f666cb296dd282b3083a031a0c3

DHA05603729805

Company Information

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.9999 Miscellaneous

import

Dates and Status

Sep 06, 2024

Jul 12, 2029