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“Genoss” GENOSS Inflator B30 and GENOSS Inflator B40 - Taiwan Registration d8cb14f0836a0be38fcaebfd45b54eaa

Access comprehensive regulatory information for “Genoss” GENOSS Inflator B30 and GENOSS Inflator B40 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8cb14f0836a0be38fcaebfd45b54eaa 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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Registration Details
Taiwan FDA Registration: d8cb14f0836a0be38fcaebfd45b54eaa
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Device Details

“Genoss” GENOSS Inflator B30 and GENOSS Inflator B40
TW: “吉諾司” 擴張壓力泵
Risk Class 2
MD

Registration Details

d8cb14f0836a0be38fcaebfd45b54eaa

Ministry of Health Medical Device Import No. 035017

DHA05603501700

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