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

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Vitalograph Model 6800 Pneumotrac

FDA 510(k)
FDA Class 2 ·Anesthesiology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526799394·MANUMED ACTIVE WRIST LEFT SAND S

Pathway

FDA UDI
SPINAL ELEMENTS·00840916129583·Pathway ELIF Small 12mm

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613021979·Guilford-Wright Wire Cutter, Serrated, 15mm Mid...

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613090784·Guilford-Wright Roller Knife, 3mm Diameter Roll...

BBLCHROMAGAR MRSA

FDA 510(k)
FDA Class 2 ·Microbiology

GAMMA-BSM; BETA-BSM; EQUIVABONE

FDA 510(k)
FDA Class 2 ·Dental

HEARTSTART FRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 24, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 30, 2014

M-1 COT KNEE GATCH LITTER

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FPO·June 20, 2011

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 29, 2020

DYB INTRODUCER, CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code DYB·November 12, 2025

FLEXOR SHUTTLE SELECT GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·January 12, 2018

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·April 19, 2021

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 15, 2020

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·January 16, 2020

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·August 15, 2019