Taiwan FDA registration 675c61de75861d7b0c0b01752814a921

Coronary artery balloon dilation catheter

TW: 冠狀動脈氣球擴張導管
Taiwan flagTaiwan·SCHNEIDER (EUROPE) GMBH·Registered Sep 03, 1999 – Oct 05, 2002Cancelled
Registration details
Analysis ID
675c61de75861d7b0c0b01752814a921
Customs Code
DHA00600929409
Company information
Manufacturer Country
Switzerland
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Sep 03, 1999
Expiry Date
Oct 05, 2002
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 Coronary artery balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 675c61de75861d7b0c0b01752814a921 and manufactured by SCHNEIDER (EUROPE) GMBH. The authorized representative in Taiwan is BOSTON SCIENTIFIC INTERNATIONAL B.V., TAIWAN BRANCH (NETHERLANDS).

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including BLUE MEDICAL DEVICES B.V., NUMED CANADA INC., 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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