Taiwan FDA registration 02eae7e85e079578dcc992a31e2f1968

Implanted cardiac rectifier

TW: 內植用心臟整律器
Taiwan flagTaiwan·CORDIS EUROPA N. V. A JOHNSON & JOHNSON CO.·Registered Jun 28, 1983 – Jun 28, 1988Cancelled
Registration details
Analysis ID
02eae7e85e079578dcc992a31e2f1968
Customs Code
DHA00600257903
Company information
Manufacturer Country
Netherlands
Authorized Representative
KENT CORPORATION
Product details
Product Type (Level 1)
0332 Implanted cardiac rhythmometer
Import Information
import
Dates and status
Registration Date
Jun 28, 1983
Expiry Date
Jun 28, 1988
Cancellation Date
Feb 26, 1990
Cancellation information
Status
Logged out
Reason
有效期限已屆
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About this record

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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