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"Biosen Webster" reservoir flow perfusion cannula set - Taiwan Registration 0c24e7010ddeb17018faa07b5d92d4d4

Access comprehensive regulatory information for "Biosen Webster" reservoir flow perfusion cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c24e7010ddeb17018faa07b5d92d4d4 and manufactured by BIOSENSE WEBSTER, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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0c24e7010ddeb17018faa07b5d92d4d4
Registration Details
Taiwan FDA Registration: 0c24e7010ddeb17018faa07b5d92d4d4
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Device Details

"Biosen Webster" reservoir flow perfusion cannula set
TW: โ€œ็™พๆญๆฃฎๅ‰ไผฏๅธ็‰นโ€ๅบซๆต็Œๆณจๅฅ—็ฎก็ต„
Risk Class 2

Registration Details

0c24e7010ddeb17018faa07b5d92d4d4

DHA00601874201

Company Information

United States

Product Details

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

J General hospital and personal use equipment

J.5440 ่ก€็ฎกๅ…ง่ผธๆถฒๅฅ—

import

Dates and Status

Mar 24, 2008

Mar 24, 2023