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"Plusrite" flow rate development ultrasound guidance for a complete set of implantable vascular infusion - Taiwan Registration ae5e7c82eac52c671b58538f8a1cb813

Access comprehensive regulatory information for "Plusrite" flow rate development ultrasound guidance for a complete set of implantable vascular infusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ae5e7c82eac52c671b58538f8a1cb813 and manufactured by PEROUSE MEDICAL. The authorized representative in Taiwan is AMED CO., LTD..

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ae5e7c82eac52c671b58538f8a1cb813
Registration Details
Taiwan FDA Registration: ae5e7c82eac52c671b58538f8a1cb813
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Device Details

"Plusrite" flow rate development ultrasound guidance for a complete set of implantable vascular infusion
TW: โ€œๆ™ฎ็พ…ๆ–ฏโ€ๆต้€Ÿ้กฏๅฝฑ่ถ…้Ÿณๆณขๅผ•ๅฐŽ็”จๅ…จๅฅ—ๅผๆคๅ…ฅๅผ่ก€็ฎก่ผธๆณจๅ™จ
Risk Class 2

Registration Details

ae5e7c82eac52c671b58538f8a1cb813

DHA05603320902

Company Information

France

Product Details

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

J General hospital and personal use equipment

import

Dates and Status

Jan 13, 2020

Jan 13, 2030