Pure Global

“Genoss” GENOSS Control Syringe - Taiwan Registration 5920a2c7be7fc546637737954d9b135a

Access comprehensive regulatory information for “Genoss” GENOSS Control Syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5920a2c7be7fc546637737954d9b135a 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
5920a2c7be7fc546637737954d9b135a
Registration Details
Taiwan FDA Registration: 5920a2c7be7fc546637737954d9b135a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Genoss” GENOSS Control Syringe
TW: “吉諾司” 可控式顯影注射器
Risk Class 2
MD

Registration Details

5920a2c7be7fc546637737954d9b135a

Ministry of Health Medical Device Import No. 035016

DHA05603501601

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

E Cardiovascular devices

E1650 Vascular photography syringes and syringes

Imported from abroad

Dates and Status

Nov 01, 2021

Nov 01, 2026