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“SEAWON” FORA-B Steerable Epidural Balloon Catheter - Taiwan Registration 03925e52b6d06bf1305b0d36ad3e7da7

Access comprehensive regulatory information for “SEAWON” FORA-B Steerable Epidural Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 03925e52b6d06bf1305b0d36ad3e7da7 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. 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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03925e52b6d06bf1305b0d36ad3e7da7
Registration Details
Taiwan FDA Registration: 03925e52b6d06bf1305b0d36ad3e7da7
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Device Details

“SEAWON” FORA-B Steerable Epidural Balloon Catheter
TW: “喜旺”佛爾畢可操控硬膜外氣球導管
Risk Class 2
MD

Registration Details

03925e52b6d06bf1305b0d36ad3e7da7

Ministry of Health Medical Device Import No. 029795

DHA05602979500

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

D Devices for anesthesiology

D5120 Anesthesia delivery catheter

Imported from abroad

Dates and Status

Jun 16, 2017

Jun 16, 2027