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"Baxter" kidney artificial kidney - Taiwan Registration 4ef8a42edc7d2fdb9a64fc27f29cb0d2

Access comprehensive regulatory information for "Baxter" kidney artificial kidney in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ef8a42edc7d2fdb9a64fc27f29cb0d2 and manufactured by NIPRO CORPORATION ODATE FACTORY;; 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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4ef8a42edc7d2fdb9a64fc27f29cb0d2
Registration Details
Taiwan FDA Registration: 4ef8a42edc7d2fdb9a64fc27f29cb0d2
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Device Details

"Baxter" kidney artificial kidney
TW: โ€œ็™พ็‰นโ€ๅˆฉ่…Žไบบๅทฅ่…Ž่‡Ÿ
Risk Class 2
Cancelled

Registration Details

4ef8a42edc7d2fdb9a64fc27f29cb0d2

DHA05602537102

Company Information

Product Details

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

H Gastroenterology and urology

H.5860 ้ซ˜ๆปฒ้€ๆ€งไน‹่ก€ๆถฒ้€ๆž็ณป็ตฑ

Chinese goods;; Input;; Contract manufacturing

Dates and Status

Aug 13, 2013

Aug 13, 2018

Aug 05, 2022

Cancellation Information

Logged out

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