27 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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