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"Kamma" blood bank centrifuge for in vitro diagnosis - Taiwan Registration 625dde95dc3bdebf76735d00eb02a5b3

Access comprehensive regulatory information for "Kamma" blood bank centrifuge for in vitro diagnosis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 625dde95dc3bdebf76735d00eb02a5b3 and manufactured by THERMO ELECTRON LED GMBH. The authorized representative in Taiwan is BIOWAY CORPORATION.

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625dde95dc3bdebf76735d00eb02a5b3
Registration Details
Taiwan FDA Registration: 625dde95dc3bdebf76735d00eb02a5b3
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Device Details

"Kamma" blood bank centrifuge for in vitro diagnosis
TW: โ€œ็ฅžๆ‘ฉโ€้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ
Risk Class 1
Cancelled

Registration Details

625dde95dc3bdebf76735d00eb02a5b3

DHA04400975207

Company Information

Germany

Product Details

Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.

B Hematology, pathology, and genetics

B.9275 Blood bank centrifuge for in vitro diagnostics

import

Dates and Status

Dec 28, 2010

Dec 28, 2015

May 21, 2018

Cancellation Information

Logged out

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