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Platyfenda angiography catheter - Taiwan Registration f3c8ba48bf8c3fb317e58abb8d39beb4

Access comprehensive regulatory information for Platyfenda angiography catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number f3c8ba48bf8c3fb317e58abb8d39beb4 and manufactured by MAXXIM MEDICAL,ARGON DIVISION. The authorized representative in Taiwan is Taiwan Bidu Squibb Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MAXXIM MEDICAL,ARGON DIVISION, and 1 recent registrations in the same category. 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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f3c8ba48bf8c3fb317e58abb8d39beb4
Registration Details
Taiwan FDA Registration: f3c8ba48bf8c3fb317e58abb8d39beb4
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Device Details

Platyfenda angiography catheter
TW: ๆŸ่Šฌ้”่ก€็ฎกๆ”ๅฝฑๅฐŽ็ฎก
Cancelled

Registration Details

f3c8ba48bf8c3fb317e58abb8d39beb4

DHA00600548305

Company Information

United States

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Feb 13, 1989

Feb 13, 1994

Jan 22, 1994

Cancellation Information

Logged out

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