Taiwan FDA registration eb4800a41c841e256ae3ba9d69274206

Cardiac rectifier

TW: 心臟整律器
Taiwan flagTaiwan·VITATRON MEDICAL B. V.·Registered Oct 21, 1981 – Oct 21, 1986Cancelled
Registration details
Analysis ID
eb4800a41c841e256ae3ba9d69274206
Customs Code
DHA00600181408
Company information
Manufacturer Country
Netherlands
Authorized Representative
TAIWAN BIOMEDICAL INSTRUMENTS LTD.
Product details
Product Type (Level 1)
0609 Extracorporeal cardiac plasticist
Import Information
import
Dates and status
Registration Date
Oct 21, 1981
Expiry Date
Oct 21, 1986
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 Cardiac rectifier in Taiwan's medical device market through Pure Global AI's free database. is registered under number eb4800a41c841e256ae3ba9d69274206 and manufactured by VITATRON MEDICAL B. V.. The authorized representative in Taiwan is TAIWAN BIOMEDICAL INSTRUMENTS LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Medtronic Inc.; Medtronic Europe Sàrl, 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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