Taiwan FDA registration 484303d1cace91d6410e79034b975469

Aortic luminal balloon pump

TW: 主動脈腔內氣球泵
Taiwan flagTaiwan·DATASCOPE CORPORATION PATIENT MONITORING DIVISION·Registered Dec 16, 1994 – Feb 09, 2004Cancelled
Registration details
Analysis ID
484303d1cace91d6410e79034b975469
Customs Code
DHA00600739202
Company information
Manufacturer Country
United States
Authorized Representative
Tai Lai Trading Company Limited
Product details
Product Type (Level 1)
0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Dec 16, 1994
Expiry Date
Feb 09, 2004
Cancellation Date
Aug 28, 2007
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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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 484303d1cace91d6410e79034b975469 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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