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"Baxter" automated peritoneal dialysis system - Taiwan Registration 8c3bd33f3c8e663a49eb92d0b62237bf

Access comprehensive regulatory information for "Baxter" automated peritoneal dialysis system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8c3bd33f3c8e663a49eb92d0b62237bf and manufactured by BAXTER HEALTHCARE S.A. 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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8c3bd33f3c8e663a49eb92d0b62237bf
Registration Details
Taiwan FDA Registration: 8c3bd33f3c8e663a49eb92d0b62237bf
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Device Details

"Baxter" automated peritoneal dialysis system
TW: "็™พ็‰น" ่‡ชๅ‹•่…น่†œ้€ๆž็ณป็ตฑ
Risk Class 2

Registration Details

8c3bd33f3c8e663a49eb92d0b62237bf

DHA00601129809

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

import

Dates and Status

May 09, 2005

May 09, 2025