Taiwan FDA registration 4fda4b2aad1e319bee4243ef621f9fef

"McKovei" aortic balloon catheter

TW: "邁柯唯"主動脈氣球導管
Taiwan flagTaiwan·Risk Class 3·DATASCOPE CORP.·Registered Mar 21, 2003 – Mar 21, 2028Active
Registration details
Analysis ID
4fda4b2aad1e319bee4243ef621f9fef
Customs Code
DHA00601024904
Company information
Manufacturer
DATASCOPE CORP.
Manufacturer Country
United States
Authorized Representative
GETINGE GROUP TAIWAN CO., LTD.
Product details
Product Type (Level 1)
E Cardiovascular Medicine Science
Import Information
import
Dates and status
Registration Date
Mar 21, 2003
Expiry Date
Mar 21, 2028
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About this record

Access comprehensive regulatory information for "McKovei" aortic balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 4fda4b2aad1e319bee4243ef621f9fef and manufactured by DATASCOPE CORP.. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DATASCOPE CORP., 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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