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"Pinabo" INTICO suction system - Taiwan Registration 31e2b56a58dfe15f3bfc17434ff5984c

Access comprehensive regulatory information for "Pinabo" INTICO suction system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 31e2b56a58dfe15f3bfc17434ff5984c and manufactured by Penumbra, Inc.. The authorized representative in Taiwan is FRONTIER BIO-MEDICAL INC..

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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31e2b56a58dfe15f3bfc17434ff5984c
Registration Details
Taiwan FDA Registration: 31e2b56a58dfe15f3bfc17434ff5984c
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Device Details

"Pinabo" INTICO suction system
TW: โ€œๅฝผๅจœๆณขโ€่‹ฑ่ฟช้ซ˜ๆŠฝๅธ็ณป็ตฑ
Risk Class 2

Registration Details

31e2b56a58dfe15f3bfc17434ff5984c

DHA05603606401

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular Medicine Science

E.5150 ่ก€ๆ “ๅˆ‡้™ค่ก“ๅฐŽ็ฎก

import

Dates and Status

Dec 14, 2022

Dec 14, 2027