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"Baxter" continuous blood purification instrument - Taiwan Registration 2ce532d8565871d58ec597ec8eae20f6

Access comprehensive regulatory information for "Baxter" continuous blood purification instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2ce532d8565871d58ec597ec8eae20f6 and manufactured by GAMBRO DASCO S.p.A.;; Baxter Healthcare SA. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GAMBRO LUNDIA AB;; GAMBRO DASCO S.p.A., and 1 recent registrations in the same category. 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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2ce532d8565871d58ec597ec8eae20f6
Registration Details
Taiwan FDA Registration: 2ce532d8565871d58ec597ec8eae20f6
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Device Details

"Baxter" continuous blood purification instrument
TW: โ€œ็™พ็‰นโ€้€ฃ็บŒๆ€ง่ก€ๆถฒๆทจๅŒ–ๅ„€ๅ™จ
Risk Class 2

Registration Details

2ce532d8565871d58ec597ec8eae20f6

DHA05603761109

Company Information

Italy;;Switzerland

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

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

import

Dates and Status

Sep 30, 2024

Sep 30, 2029

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