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“Cryotech”Cell-freezing apparatus and reagents for in vitro diagnostic use (Non-Sterile) - Taiwan Registration 0b51f73db1dbcb1af0ec225b53ce6c1d

Access comprehensive regulatory information for “Cryotech”Cell-freezing apparatus and reagents for in vitro diagnostic use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0b51f73db1dbcb1af0ec225b53ce6c1d and manufactured by REPROLIFE INC.. The authorized representative in Taiwan is LabIVF Taiwan International Co., Ltd.

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0b51f73db1dbcb1af0ec225b53ce6c1d
Registration Details
Taiwan FDA Registration: 0b51f73db1dbcb1af0ec225b53ce6c1d
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Device Details

“Cryotech”Cell-freezing apparatus and reagents for in vitro diagnostic use (Non-Sterile)
TW: “磊柏”體外診斷用的細胞冷凍設備及反應劑 (未滅菌)
Risk Class 1
MD

Registration Details

0b51f73db1dbcb1af0ec225b53ce6c1d

Ministry of Health Medical Device Import No. 022158

DHA09402215804

Company Information

Japan

Product Details

Limited to the first level identification range of cell cryogenic equipment and reactants (B.9225) for in vitro diagnosis of medical device management methods.

B Hematology and pathology devices

B9225 Cell cryogenic equipment and reactants for in vitro diagnostics

Imported from abroad

Dates and Status

Dec 04, 2020

Dec 04, 2025