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"Kabi" Ajili infusion pump - Taiwan Registration 5df12c75b3dcd251a494bf932d46652d

Access comprehensive regulatory information for "Kabi" Ajili infusion pump in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5df12c75b3dcd251a494bf932d46652d 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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5df12c75b3dcd251a494bf932d46652d
Registration Details
Taiwan FDA Registration: 5df12c75b3dcd251a494bf932d46652d
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Device Details

"Kabi" Ajili infusion pump
TW: โ€œๅกๆฏ”โ€่‰พๆท่މ่ผธๆถฒๅนซๆตฆ
Risk Class 2

Registration Details

5df12c75b3dcd251a494bf932d46652d

DHA05603089501

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

May 16, 2018

May 16, 2028