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"Kabi" Wei all-round infusion system software - Taiwan Registration 579c9bafc2d7c2412b9fa003bfc8ac3b

Access comprehensive regulatory information for "Kabi" Wei all-round infusion system software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 579c9bafc2d7c2412b9fa003bfc8ac3b and manufactured by Fresenius Vial S.A.S.;; Fresenius Kabi AG. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

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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579c9bafc2d7c2412b9fa003bfc8ac3b
Registration Details
Taiwan FDA Registration: 579c9bafc2d7c2412b9fa003bfc8ac3b
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Device Details

"Kabi" Wei all-round infusion system software
TW: โ€œๅกๆฏ”โ€ๅจๅ…จ่ƒฝ่ผธๆถฒ็ณป็ตฑ่ปŸ้ซ”
Risk Class 2

Registration Details

579c9bafc2d7c2412b9fa003bfc8ac3b

DHA05603394801

Company Information

Product Details

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

J General hospital and personal use equipment

J.5725 Infusion ๅนซๆตฆ

import

Dates and Status

Sep 10, 2020

Sep 10, 2025