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"New Foden" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration c0d7f3682d3c29b352f22a866ca7484b

Access comprehensive regulatory information for "New Foden" blood bank centrifuge for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c0d7f3682d3c29b352f22a866ca7484b and manufactured by SILFRADENT SRL. The authorized representative in Taiwan is DENTWEI INDUSTRY CO., LTD..

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c0d7f3682d3c29b352f22a866ca7484b
Registration Details
Taiwan FDA Registration: c0d7f3682d3c29b352f22a866ca7484b
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Device Details

"New Foden" blood bank centrifuge for in vitro diagnostics (unsterilized)
TW: โ€œๆ–ฐ็ฆ็™ปโ€้ซ”ๅค–่จบๆ–ท็”จ่ก€ๅบซ้›ขๅฟƒๆฉŸ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

c0d7f3682d3c29b352f22a866ca7484b

DHA04401199308

Company Information

Italy

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

Input;; QMS/QSD

Dates and Status

Jul 30, 2012

Jul 30, 2017

Dec 20, 2019

Cancellation Information

Logged out

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