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“SEAWON” Veeler Video Guided Catheter - Taiwan Registration 4ffe7ea5e23934ff39641353f0ab0bcb

Access comprehensive regulatory information for “SEAWON” Veeler Video Guided Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ffe7ea5e23934ff39641353f0ab0bcb and manufactured by SEAWON MEDITECH CO., LTD.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Seawon Meditech Co., Ltd., 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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4ffe7ea5e23934ff39641353f0ab0bcb
Registration Details
Taiwan FDA Registration: 4ffe7ea5e23934ff39641353f0ab0bcb
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Device Details

“SEAWON” Veeler Video Guided Catheter
TW: “喜旺”米勒影像引導導管
Risk Class 2
MD
Cancelled

Registration Details

4ffe7ea5e23934ff39641353f0ab0bcb

Ministry of Health Medical Device Import No. 027587

DHA05602758706

Company Information

Korea, Republic of

Product Details

D Devices for anesthesiology

D5120 Anesthesia delivery catheter

Imported from abroad

Dates and Status

Aug 10, 2015

Aug 10, 2020

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者

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