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"Fresenius" blood cell separator cannula set - Taiwan Registration 5e571e267b7ce7de693b7af3febb4c93

Access comprehensive regulatory information for "Fresenius" blood cell separator cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e571e267b7ce7de693b7af3febb4c93 and manufactured by FRESENIUS KABI AG;; FRESENIUS HEMOCARE NETHERLANDS B.V.. The authorized representative in Taiwan is Fresenius Kabi, Taiwan Co., 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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5e571e267b7ce7de693b7af3febb4c93
Registration Details
Taiwan FDA Registration: 5e571e267b7ce7de693b7af3febb4c93
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Device Details

"Fresenius" blood cell separator cannula set
TW: โ€œ่ฒปๆฃฎๅฐคๆ–ฏโ€่ก€ๆถฒ็ดฐ่ƒžๅˆ†้›ขๅ™จๅฅ—็ฎก็ต„
Risk Class 2
Cancelled

Registration Details

5e571e267b7ce7de693b7af3febb4c93

DHA00601929800

Company Information

Product Details

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

B Hematology, pathology, and genetics

B.9100 Containers for the collection and disposal of blood and blood components

import

Dates and Status

Oct 27, 2008

Oct 27, 2013

Apr 09, 2015

Cancellation Information

Logged out

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