35 results · 25ms · Sources: EU EUDAMED, US FDA

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CAPINTEC CRC 55T SERIES DOSE CALIBRATORS, MODELS CRC 55TR, CRC 55TPET AND CRC 55TW

FDA 510(k)
FDA Class 2 ·Radiology

HHM

FDA UDI
Oticon A/S·05707131164469·K140, BTE 13 CNB HHM

GPAC II KNEE SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304184596·

Welch Allyn, Inc.

FDA UDI
WELCH ALLYN, INC.·00732094070132·Welch Allyn CardioPerfect Workstation with PC-B...

NITANIUM® SUPER ELASTIC ARCHWIRES

FDA UDI
Ortho Organizers, Inc.·00190707060312·.021 X .025 UPPER NITANIUM® SUPER ELASTIC OVAL ...

ENDOSKELETON® TAS

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00191375032120·Rigid Container System, Tray

OMNI III PATIENT MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

CAVEX STABISIL

FDA 510(k)
FDA Class 2 ·Dental

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 32 SIZE M

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 26, 2023

ACCELSTIM

FDA Adverse Event
Injury ·ORTHOFIX·Product code LOF·June 5, 2023

PAINSMART IOD

FDA Adverse Event
Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 30, 2013

GRANUFLO

FDA Adverse Event
Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 24, 2011

CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·August 14, 2017

CANTATA 2.8 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·November 17, 2017

CANTATA 2.5 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·September 17, 2018

CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·September 11, 2018

CANTATA 2.5 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·July 28, 2017

CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·June 15, 2017

CANTATA 2.5 SUPERSELECTIVE MICROCATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·May 30, 2018