Implanted cardiac rectifier
Taiwan·CORDIS CORPORATION·Registered Jan 08, 1988 – Jan 08, 1993Cancelled- Analysis ID
- a59095a88f418528679bfb3c053b95fa
- Customs Code
- DHA00600498205
- Manufacturer
- CORDIS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- KENT CORPORATION
- Product Type (Level 1)
- 0332 Implanted cardiac rhythmometer
- Import Information
- import
- Registration Date
- Jan 08, 1988
- Expiry Date
- Jan 08, 1993
- Cancellation Date
- Nov 01, 1999
- Status
- Logged out
- Reason
- 未展延而逾期者;;改列無須辦理查驗之醫療器材
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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.