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“Genoss” Extractor Aspiration Catheter - Taiwan Registration a9a4deecb08764f5dd03939d09e2d76b

Access comprehensive regulatory information for “Genoss” Extractor Aspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a9a4deecb08764f5dd03939d09e2d76b 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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a9a4deecb08764f5dd03939d09e2d76b
Registration Details
Taiwan FDA Registration: a9a4deecb08764f5dd03939d09e2d76b
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Device Details

“Genoss” Extractor Aspiration Catheter
TW: “吉諾司”血栓清除導管
Risk Class 2
MD

Registration Details

a9a4deecb08764f5dd03939d09e2d76b

Ministry of Health Medical Device Import No. 033088

DHA05603308800

Company Information

Korea, Republic of

Product Details

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

E Cardiovascular devices

E5150 Thrombectomy catheter

Imported from abroad

Dates and Status

Jan 10, 2020

Jan 10, 2025