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“JMS” HemoPress Automated blood component separator - Taiwan Registration c31e113e3a565c4fd660fbab4c947f61

Access comprehensive regulatory information for “JMS” HemoPress Automated blood component separator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c31e113e3a565c4fd660fbab4c947f61 and manufactured by JMS SINGAPORE PTE LTD.. The authorized representative in Taiwan is EXCELSIOR MEDICAL CO., LTD..

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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c31e113e3a565c4fd660fbab4c947f61
Registration Details
Taiwan FDA Registration: c31e113e3a565c4fd660fbab4c947f61
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Device Details

“JMS” HemoPress Automated blood component separator
TW: “杰斯”自動壓板機
Risk Class 2
MD
Cancelled

Registration Details

c31e113e3a565c4fd660fbab4c947f61

Ministry of Health Medical Device Import No. 028428

DHA05602842804

Company Information

Singapore

Product Details

B Hematology and pathology devices

B0002 Blood component extraction device

Imported from abroad

Dates and Status

May 26, 2016

May 26, 2021

Sep 08, 2023

Cancellation Information

Logged out

未展延而逾期者