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"TERUMO" TERUFUSION SOLUTION ADMINISTRATION SET - Taiwan Registration 4082566e2455f0f235f4c8b257634300

Access comprehensive regulatory information for "TERUMO" TERUFUSION SOLUTION ADMINISTRATION SET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4082566e2455f0f235f4c8b257634300 and manufactured by KOFU FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN 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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4082566e2455f0f235f4c8b257634300
Registration Details
Taiwan FDA Registration: 4082566e2455f0f235f4c8b257634300
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Device Details

"TERUMO" TERUFUSION SOLUTION ADMINISTRATION SET
TW: ่ผธๆถฒๅฅ—
Risk Class 2
MD

Registration Details

4082566e2455f0f235f4c8b257634300

Department of Health Medical Device Import No. 007673

DHA00600767307

Company Information

Product Details

1399 Other blood transfusion, infusion equipment

Imported from abroad

Dates and Status

Aug 02, 1999

Nov 21, 2025