Taiwan FDA registration 625dde95dc3bdebf76735d00eb02a5b3
"Kamma" blood bank centrifuge for in vitro diagnosis
TW: “神摩”體外診斷用血庫離心機
Taiwan·Risk Class 1·THERMO ELECTRON LED GMBH·Registered Dec 28, 2010 – Dec 28, 2015CancelledRegistration details
- Analysis ID
- 625dde95dc3bdebf76735d00eb02a5b3
- Customs Code
- DHA04400975207
Company information
- Manufacturer
- THERMO ELECTRON LED GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- BIOWAY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.9275 Blood bank centrifuge for in vitro diagnostics
- Import Information
- import
Dates and status
- Registration Date
- Dec 28, 2010
- Expiry Date
- Dec 28, 2015
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
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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