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"Baxter" fully automated peritoneal dialysis tube set - Taiwan Registration 9a483a9d2b4bc346a798b8fe511bd383

Access comprehensive regulatory information for "Baxter" fully automated peritoneal dialysis tube set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a483a9d2b4bc346a798b8fe511bd383 and manufactured by BAXTER HEALTHCARE SA, SINGAPORE BRANCH. The authorized representative in Taiwan is BAXTER HEALTHCARE 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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9a483a9d2b4bc346a798b8fe511bd383
Registration Details
Taiwan FDA Registration: 9a483a9d2b4bc346a798b8fe511bd383
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Device Details

"Baxter" fully automated peritoneal dialysis tube set
TW: "็™พ็‰น" ๅ…จ่‡ชๅ‹•่…น่†œ้€ๆž็ฎก็ต„
Risk Class 2

Registration Details

9a483a9d2b4bc346a798b8fe511bd383

DHA00601041702

Company Information

Product Details

H Gastroenterology and urology

import

Dates and Status

Sep 30, 2003

Sep 30, 2028