10 results
·
54ms
·
Sources: EU EUDAMED, US FDA
CULTURETTE, S/P BRAND
FDA Adverse Event
Malfunction
·BAXTER DIAGNOSTICS, INC.·Product code JSC·March 17, 1994
DACII AUTOMATIC CENTRIFUGE
FDA Adverse Event
Malfunction
·BAXTER DIAGNOSTICS, INC.·Product code JQC·March 8, 1995
AUTOMATED CHEM SYSTEM
FDA Adverse Event
BAXTER DIAGNOSTICS, INC.·Product code JJC·November 10, 1994
BAXTER
FDA Adverse Event
Injury
·BAXTER DIAGNOSTICS, INC. PRODUCT SVC MGMT·Product code FRN·May 31, 2001
DIASCAN TEST STRIPS
FDA Adverse Event
Injury
·HOME DIAGNOSTICS, INC.·Product code CFR·January 28, 1993
SYNDEO SYRINGE PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FRN·November 18, 2009
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 10, 2010
BAXTER DIAGNOSTICS
FDA Adverse Event
Malfunction
·DADE BEHRING, INC. (BAXTER DIAGNOSTICS)·Product code FRN·January 24, 2000
BAXTER
FDA Adverse Event
Malfunction
·BAXER DIAGNOSTICS, INC. PRODUCT SVC MGMT·Product code FRN·October 22, 2001
Obelis s.a.
Authorized representative
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