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"Otto" myocardial lead - Taiwan Registration fb14c8220f8d0d3348e0c72f281aa674

Access comprehensive regulatory information for "Otto" myocardial lead in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fb14c8220f8d0d3348e0c72f281aa674 and manufactured by ALTO DEVELOPMENT CORPORATION. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN 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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fb14c8220f8d0d3348e0c72f281aa674
Registration Details
Taiwan FDA Registration: fb14c8220f8d0d3348e0c72f281aa674
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Device Details

"Otto" myocardial lead
TW: "ๅฅงๅœ–" ๅฟƒ่‚ŒๅฐŽ็ทš
Risk Class 2

Registration Details

fb14c8220f8d0d3348e0c72f281aa674

DHA00600982705

Company Information

United States

Product Details

Vacuum.

E Cardiovascular Medicine Science

Dates and Status

Feb 19, 2002

Feb 19, 2027