14 results · 49ms · Sources: EU EUDAMED, US FDA

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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