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"TERUMO" CDI SHUNT SENSOR - Taiwan Registration 6423568ccdcef44e32c39abbb22b2425

Access comprehensive regulatory information for "TERUMO" CDI SHUNT SENSOR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6423568ccdcef44e32c39abbb22b2425 and manufactured by TERUMO CARDIOVASCULAR SYSTEMS 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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6423568ccdcef44e32c39abbb22b2425
Registration Details
Taiwan FDA Registration: 6423568ccdcef44e32c39abbb22b2425
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Device Details

"TERUMO" CDI SHUNT SENSOR
TW: ๅˆ†ๆตๆ„Ÿ็Ÿฅๅ™จ
Risk Class 2
MD

Registration Details

6423568ccdcef44e32c39abbb22b2425

Department of Health Medical Device Import No. 009351

DHA00600935108

Company Information

Product Details

1399 Other blood transfusion, infusion equipment

Imported from abroad

Dates and Status

Dec 28, 1999

Feb 09, 2029