14 results
·
49ms
·
Sources: EU EUDAMED, US FDA
BEHRING FIBRINTIMER A
FDA Adverse Event
Injury
·BEHRING DIAGNOSTICS, INC.·Product code GKT·July 1, 1997
FIBRINTIMER A COAGULATION ANALYZER
FDA Adverse Event
Malfunction
·BEHRING DIAGNOSTICS, INC.·Product code JPA·March 28, 1996
BEHRING FIBRINTIMER A
FDA Adverse Event
Injury
·BEHRING DIAGNOSTIC, INC.·Product code GKT·July 1, 1997
BFA
FDA Adverse Event
Injury
·BEHRING DIAGNOSTIC, INC.·Product code GKT·July 1, 1997
BEHRING FIBRINTIMER A
FDA Adverse Event
Injury
·BEHRING DIAGNOSTIC, INC.·Product code GKT·July 1, 1997
BEHRING FIBRINTIMER A
FDA Adverse Event
Injury
·BEHRING DIAGNOSTIC, INC.·Product code GKT·July 1, 1997
BEHRING FIBRINTIMER A
FDA Adverse Event
Injury
·BEHRING DIAGNOSTIC, INC.·Product code GKT·July 1, 1997
SYSMEX CA-1500 ANALYZER
FDA Adverse Event
Other
·SYSMEX CORPORATION·Product code GKP·April 11, 2014
BAXTER DIAGNOSTICS
FDA Adverse Event
Malfunction
·DADE BEHRING, INC. (BAXTER DIAGNOSTICS)·Product code FRN·January 24, 2000
Site Rite Vision Ultrasound System, REF 9770032, Bard Access Systems, Inc. Intended for diagnostic ultrasound imaging or fluid flow analysis of the human body.
FDA Recall
Terminated
·Bard Access Systems·Product code IYN·June 21, 2011
Precedence SPECT/CT System, Precedence 16 3/8, Upper Patient Pallet, A single photon nuclear medicine and image from an X-ray computed tomography system, Model Number: 4535 602 50851, Catalog Number: 882350, Product is manufactured by Philips Medical Systems (Cleveland), Inc. Cleveland, OH Intended use: A single photon nuclear medicine and image from an X-ray computed tomography system.
FDA Recall
Terminated
·Phillips Nuclear Medicine·Product code INQ·January 26, 2009
MDSS GmbH
Authorized representative
🇩🇪 Germany·388 Manufacturers·16562 Devices
Advena Limited
Authorized representative
🇲🇹 Malta·467 Manufacturers·13717 Devices
SUNGO Europe B.V.
Authorized representative
🇳🇱 Netherlands·1571 Manufacturers·20390 Devices