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"Bevier" blood concentrator - Taiwan Registration 1832dcc7cb4009d564a733c5c2ba7780

Access comprehensive regulatory information for "Bevier" blood concentrator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1832dcc7cb4009d564a733c5c2ba7780 and manufactured by 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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1832dcc7cb4009d564a733c5c2ba7780
Registration Details
Taiwan FDA Registration: 1832dcc7cb4009d564a733c5c2ba7780
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Device Details

"Bevier" blood concentrator
TW: "ๆฏ”ๅญš"่ก€ๆถฒๆฟƒ็ธฎๅ™จ
Risk Class 2
Cancelled

Registration Details

1832dcc7cb4009d564a733c5c2ba7780

DHA00601696406

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Aug 04, 2006

Aug 04, 2016

Apr 25, 2018

Cancellation Information

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