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Implanted cardiac rectifier - Taiwan Registration 02eae7e85e079578dcc992a31e2f1968

Access comprehensive regulatory information for Implanted cardiac rectifier in Taiwan's medical device market through Pure Global AI's free database. is registered under number 02eae7e85e079578dcc992a31e2f1968 and manufactured by CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.. The authorized representative in Taiwan is KENT CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including CORDIS CORPORATION, GUIDANT-CARDIAC PACEMAKERS, 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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02eae7e85e079578dcc992a31e2f1968
Registration Details
Taiwan FDA Registration: 02eae7e85e079578dcc992a31e2f1968
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Device Details

Implanted cardiac rectifier
TW: ๅ…งๆค็”จๅฟƒ่‡Ÿๆ•ดๅพ‹ๅ™จ
Cancelled

Registration Details

02eae7e85e079578dcc992a31e2f1968

DHA00600257903

Company Information

Product Details

0332 Implanted cardiac rhythmometer

import

Dates and Status

Jun 28, 1983

Jun 28, 1988

Feb 26, 1990

Cancellation Information

Logged out

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