48 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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osteoSPAN Morpheus
FDA 510(k)
FDA Class 2
·Orthopedic
CPAP Filter
FDA UDI
SUNSET HEALTHCARE SOLUTIONS, INC.·00848530098759·Ultra Fine Filter Respironics DreamStation 2 Di...
CPAP Filter
FDA UDI
SUNSET HEALTHCARE SOLUTIONS, INC.·00848530098766·Ultra Fine Filter Respironics DreamStation 2 Di...
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A14282880·14mm H x 28mm W x 28mm L x 8 degrees ALIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A142828120·14mm H x 28mm W x 28mm L x 12 degrees ALIF
Yellowstone
FDA UDI
SUMMIT SPINE LLC·B587A142828150·14mm H x 28mm W x 28mm L x 15 degrees ALIF
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KWP·March 31, 2016
OBTURA GUTTA PERCHA DELIVERY SYSTEM, MODEL 823-700
FDA 510(k)
FDA Class 1
·Dental
REVIVE INTERMEDIATE CATHETER (REVIVE IC)
FDA 510(k)
FDA Class 2
·Cardiovascular
FLEXOR RTPS GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·February 27, 2020
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 3, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 30, 2014
S-ROM*LINR LSER,10 DEG,32MM C
FDA Adverse Event
Injury
·DEPUY IRELAND·Product code KWA·June 23, 2011
90 DEGREE CONTRA ANGLE SCREWDRIVER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·March 6, 2017
90 DEGREE CONTRA ANGLE SCREWDRIVER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·December 1, 2016
BIOMET MICROFIXATION FACIAL PLATING SYSTEM
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·April 25, 2017
90 DEG CONTRA ANGLE SCREWDRIVER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·October 14, 2016
90 DEGREE CONTRA ANGLE SCREWDRIVER
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·October 21, 2016
BIOMNET MICROFIXATION FACIAL PLATING SYSTEM
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code HRS·September 23, 2016
FLEXOR SHUTTLE TIBIAL GUIDING SHEATH
FDA Adverse Event
Malfunction
·COOK INC·Product code DYB·September 29, 2020