24 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATRICLIP GILLINOV-COSGROVE LAA CLIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OneLIF™
FDA UDI
Novapproach Spine LLC·G07001191311070·Bullet Trial, 11 mm AH - 07 mm PH
TALOS®-C HA
FDA UDI
MEDITECH SPINE, LLC·B167521311070·
OneLIF™
FDA UDI
Novapproach Spine LLC·G070SPX01161311070·Special Instrument Starter Trial, Medium, 13deg...
MSA HIP SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE
FDA 510(k)
FDA Class 2
·Dental
KIWI VACUUM ASSISTED FETAL DELIVERY
FDA Adverse Event
Malfunction
·CLINICAL INNOVATIONS, INC.·Product code HDB·January 23, 2014
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004906·CONTINUOUS SUCTION REGULATORS
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004944·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004920·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004913·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004937·CONTINUOUS SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004951·CONTINUOUS SUCTION REGULATORS
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
DIGITAL RADIOGRAPHY CXDI
FDA Adverse Event
Malfunction
·CANON, INC.·Product code MQB·December 22, 2019
BI-LEVEL/CPAP INSPIRATORY HEATED CIRCUIT
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·April 7, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 1, 2014
INOMAX DSIR (DELIVERY SYSTEM)
FDA Adverse Event
Injury
·IKARIA·Product code MRN·May 23, 2013
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - BUFFALO GROVE·Product code FRN·June 16, 2011