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"Baxter" automatic peritoneal dialysis machine connection platform - Taiwan Registration 8253cd12033512eaf2b26a1b3be74c41

Access comprehensive regulatory information for "Baxter" automatic peritoneal dialysis machine connection platform in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8253cd12033512eaf2b26a1b3be74c41 and manufactured by Baxter Healthcare Corporation Medical Products;; Baxter Healthcare SA. 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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8253cd12033512eaf2b26a1b3be74c41
Registration Details
Taiwan FDA Registration: 8253cd12033512eaf2b26a1b3be74c41
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Device Details

"Baxter" automatic peritoneal dialysis machine connection platform
TW: โ€œ็™พ็‰นโ€ๅ…จ่‡ชๅ‹•่…น่†œ้€ๆžๆฉŸ้€ฃ็ทšๅนณๅฐ
Risk Class 2

Registration Details

8253cd12033512eaf2b26a1b3be74c41

DHA05603034709

Company Information

Product Details

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

H Gastroenterology and urology

H.5630 ่…น่†œ้€ๆž็ณป็ตฑๅŠๅ…ถ้™„ไปถ

Contract manufacturing;; input

Dates and Status

Oct 16, 2017

Oct 16, 2027