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Balloon dilation catheter - Taiwan Registration edc5df8117e50cda83ce212b2959501a

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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edc5df8117e50cda83ce212b2959501a
Registration Details
Taiwan FDA Registration: edc5df8117e50cda83ce212b2959501a
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Device Details

Balloon dilation catheter
TW: ๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Cancelled

Registration Details

edc5df8117e50cda83ce212b2959501a

DHA00600791301

Company Information

United States

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Jul 01, 1996

Jul 01, 2001

Dec 01, 2004

Cancellation Information

Logged out

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