Taiwan FDA registration edc5df8117e50cda83ce212b2959501a

Balloon dilation catheter

TW: 氣球擴張導管
Taiwan flagTaiwan·LEOCOR, INC.·Registered Jul 01, 1996 – Jul 01, 2001Cancelled
Registration details
Analysis ID
edc5df8117e50cda83ce212b2959501a
Customs Code
DHA00600791301
Company information
Manufacturer
LEOCOR, INC.
Manufacturer Country
United States
Authorized Representative
Taiwan AsiaSatellite Co., Ltd
Product details
Product Type (Level 1)
0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
Import Information
import
Dates and status
Registration Date
Jul 01, 1996
Expiry Date
Jul 01, 2001
Cancellation Date
Dec 01, 2004
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for Balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number edc5df8117e50cda83ce212b2959501a and manufactured by LEOCOR, INC.. The authorized representative in Taiwan is Taiwan AsiaSatellite Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including TERUMO CORPORATION;; ASHITAKA FACTORY OF TERUMO CORPORATION, C.R. BARD IRELAND LTD., 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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