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Hettich Instruments Management I

4 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Mikro 12-24 Centrifuge with 2050 Rotor TYP #2070 and TYP 2070-01. Used for the purpose of recall (Z-0612-2010)Hettich Instruments Management I2010-01-21
Haematokrit 24 Centrifuge with 2050 Rotor TYP #2075 and TYP #2075-01. Used for the purpose recall (Z-0613-2010)Hettich Instruments Management I2010-01-21
Mikro 20 Centrifuge with 2076 Rotor TYP #2004 and TYP #2004-01. Used for the purpose of de recall (Z-0614-2010)Hettich Instruments Management I2010-01-21
Haematokrit 20 Centrifuge with 2050 Rotor TYP #2014-01 and TYP#201424-01. Used for the pur recall (Z-0615-2010)Hettich Instruments Management I2010-01-21

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