Taiwan FDA registration 04e94f1dc599edd730a6587fbdd30ec9

Aortic luminal balloon pump

TW: 主動脈腔內氣球泵
Taiwan flagTaiwan·DATASCOPE CORPORATION PATIENT MONITORING DIVISION·Registered Jun 02, 1981 – Jun 02, 1990Cancelled
Registration details
Analysis ID
04e94f1dc599edd730a6587fbdd30ec9
Customs Code
DHA00600172700
Company information
Manufacturer Country
United States
Authorized Representative
Tai Lai Trading Company Limited
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Jun 02, 1981
Expiry Date
Jun 02, 1990
Cancellation Date
Jul 14, 1992
Cancellation information
Status
Logged out
Reason
有效期間已屆未能補件
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About this record

Access comprehensive regulatory information for Aortic luminal balloon pump in Taiwan's medical device market through Pure Global AI's free database. is registered under number 04e94f1dc599edd730a6587fbdd30ec9 and manufactured by DATASCOPE CORPORATION PATIENT MONITORING DIVISION. The authorized representative in Taiwan is Tai Lai Trading Company Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DATASCOPE CORPORATION PATIENT MONITORING DIVISION, and 1 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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