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uTASWako i30

FUJIFILM WAKO PURE CHEMICAL CORPORATION · Model 991-60301 · UDI-DI 00856626006229

OUE Prescription
1
510(k) clearances
0
Adverse events
2
Recalls
4
Facilities

Description

In-Vitro Diagnostic Use

Recalls

DateFirmReason
2013-09-11Leica Microsystems, Inc.The ceiling mount supplier encountered an event in which the drive screw in the motor unit, which lifts and lowers the lower lift arm, broke. As a result, the lift arm fell down ap
2013-09-11Leica Microsystems, Inc.The ceiling mount supplier encountered an event in which the drive screw in the motor unit, which lifts and lowers the lower lift arm, broke. As a result, the lift arm fell down ap

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.