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"Plusrite" ultrasound guidance for a complete set of implantable vascular infusion - Taiwan Registration 6efb4c5e9b122f34846c55113bebffcb

Access comprehensive regulatory information for "Plusrite" 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 6efb4c5e9b122f34846c55113bebffcb and manufactured by PEROUSE MEDICAL. The authorized representative in Taiwan is AMED CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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6efb4c5e9b122f34846c55113bebffcb
Registration Details
Taiwan FDA Registration: 6efb4c5e9b122f34846c55113bebffcb
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Device Details

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

Registration Details

6efb4c5e9b122f34846c55113bebffcb

DHA05602582206

Company Information

France

Product Details

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

J General hospital and personal use equipment

J.5965 Subcutaneous implantable intravascular injection port and guide

import

Dates and Status

Feb 24, 2014

Feb 24, 2029