Taiwan FDA registration 36c59dd59d957f0b6ce3eb7091656280

Coronary artery balloon dilation catheter

TW: 冠狀動脈氣球擴張導管
Taiwan flagTaiwan·SCHNEIDER (EUROPE) GMBH·Registered Oct 05, 1992 – Oct 05, 2002Cancelled
Registration details
Analysis ID
36c59dd59d957f0b6ce3eb7091656280
Customs Code
DHA00600677905
Company information
Manufacturer Country
Switzerland
Authorized Representative
WATTCAN INSTRUMENTS CO., LTD.
Product details
Product Type (Level 1)
0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Oct 05, 1992
Expiry Date
Oct 05, 2002
Cancellation Date
Sep 16, 1999
Cancellation information
Status
Logged out
Reason
製造廠名稱變更;;移轉(申請商)
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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 36c59dd59d957f0b6ce3eb7091656280 and manufactured by SCHNEIDER (EUROPE) GMBH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including BLUE MEDICAL DEVICES B.V., SCHNEIDER (EUROPE) GMBH, 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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