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Implanted cardiac rectifier - Taiwan Registration a59095a88f418528679bfb3c053b95fa

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 a59095a88f418528679bfb3c053b95fa and manufactured by CORDIS CORPORATION. The authorized representative in Taiwan is KENT CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including GUIDANT-CARDIAC PACEMAKERS, CORDIS CORPORATION, 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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a59095a88f418528679bfb3c053b95fa
Registration Details
Taiwan FDA Registration: a59095a88f418528679bfb3c053b95fa
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Device Details

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

Registration Details

a59095a88f418528679bfb3c053b95fa

DHA00600498205

Company Information

United States

Product Details

0332 Implanted cardiac rhythmometer

import

Dates and Status

Jan 08, 1988

Jan 08, 1993

Nov 01, 1999

Cancellation Information

Logged out

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