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Coronary artery balloon dilation catheter - Taiwan Registration 36c59dd59d957f0b6ce3eb7091656280

Access comprehensive regulatory information for Coronary artery balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 36c59dd59d957f0b6ce3eb7091656280 and manufactured by SCHNEIDER (EUROPE) GMBH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including BLUE MEDICAL DEVICES B.V., SCHNEIDER (EUROPE) GMBH, and 5 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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36c59dd59d957f0b6ce3eb7091656280
Registration Details
Taiwan FDA Registration: 36c59dd59d957f0b6ce3eb7091656280
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Device Details

Coronary artery balloon dilation catheter
TW: ๅ† ็‹€ๅ‹•่„ˆๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Cancelled

Registration Details

36c59dd59d957f0b6ce3eb7091656280

DHA00600677905

Company Information

Switzerland

Product Details

0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment

import

Dates and Status

Oct 05, 1992

Oct 05, 2002

Sep 16, 1999

Cancellation Information

Logged out

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