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“Genoss” Initiator Angiographic Catheter - Taiwan Registration f3113f4c1c3dd5f086240acdda381752

Access comprehensive regulatory information for “Genoss” Initiator Angiographic Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3113f4c1c3dd5f086240acdda381752 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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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f3113f4c1c3dd5f086240acdda381752
Registration Details
Taiwan FDA Registration: f3113f4c1c3dd5f086240acdda381752
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Device Details

“Genoss” Initiator Angiographic Catheter
TW: “吉諾司”血管攝影導管
Risk Class 2
MD

Registration Details

f3113f4c1c3dd5f086240acdda381752

Ministry of Health Medical Device Import No. 033048

DHA05603304801

Company Information

Korea, Republic of

Product Details

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

E Cardiovascular devices

E1200 Diagnostic endovascular catheter

Imported from abroad

Dates and Status

Nov 29, 2019

Nov 29, 2024