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“Vial” Volumat Agilia Volumetric Infusion Pump - Taiwan Registration fd61aa49a7aaaf7af0e95d7a338b192b

Access comprehensive regulatory information for “Vial” Volumat Agilia Volumetric 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 fd61aa49a7aaaf7af0e95d7a338b192b and manufactured by FRESENIUS VIAL. 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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fd61aa49a7aaaf7af0e95d7a338b192b
Registration Details
Taiwan FDA Registration: fd61aa49a7aaaf7af0e95d7a338b192b
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Device Details

“Vial” Volumat Agilia Volumetric Infusion Pump
TW: “維爾”路美艾捷莉輸液幫浦
Risk Class 2
MD
Cancelled

Registration Details

fd61aa49a7aaaf7af0e95d7a338b192b

Ministry of Health Medical Device Import No. 026606

DHA05602660605

Company Information

France

Product Details

J General hospital and personal use equipment

J5725 Infusion pump

Imported from abroad

Dates and Status

Sep 09, 2014

Sep 09, 2019

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者