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“SEAWON” FORA-B TF Transforaminal Epidural Balloon Catheter System - Taiwan Registration b6ce2b3d03fa13a806c10ef5ea084a8b

Access comprehensive regulatory information for “SEAWON” FORA-B TF Transforaminal Epidural Balloon Catheter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b6ce2b3d03fa13a806c10ef5ea084a8b 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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b6ce2b3d03fa13a806c10ef5ea084a8b
Registration Details
Taiwan FDA Registration: b6ce2b3d03fa13a806c10ef5ea084a8b
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Device Details

“SEAWON” FORA-B TF Transforaminal Epidural Balloon Catheter System
TW: “喜旺”佛爾畢經椎間孔硬膜外球囊導管組
Risk Class 2
MD

Registration Details

b6ce2b3d03fa13a806c10ef5ea084a8b

Ministry of Health Medical Device Import No. 033077

DHA05603307708

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

Dec 26, 2019

Dec 26, 2024