22 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen Cannula
FDA 510(k)
FDA Class 2
·Anesthesiology
ProLift Trial
FDA UDI
Life Spine, Inc.·00190837088385·
PAGODA
FDA Adverse Event
Injury
·ORTHO DEVELOPMENT·Product code NKB·September 21, 2020
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311515060·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321515060·
VACUTRON
FDA UDI
Allied Medical, LLC·00026072004166·MINI-VAC
LUX1540, LUX1440 & LUX2940 LASER HANDPIECES
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MIELO-CAN, BEST-LISAS, BEN - BONE BIOPSY. FAST-CUT, COLT, SPRING-CUT, BIO-CUT - SOFT TISSUE BIOPSY
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008416·CONTINUOUS INTERMITTENT SUCTION REGULATORS
LUX 1440
FDA Adverse Event
Malfunction
·PALOMAR MEDICAL TECHNOLOGIES, INC.·Product code GEX·May 5, 2012
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008461·CONTINUOUS INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008423·CONTINUOUS INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008454·CONTINUOUS INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008430·CONTINUOUS INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072008447·CONTINUOUS INTERMITTENT SUCTION REGULATORS
S3 EX - 3005
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 7, 2013
PARADYM
FDA Adverse Event
Malfunction
·SORIN CRM S.R.L.·Product code MRM·June 24, 2011
VERSACARE
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·September 10, 2008
ENDOSKELETON® TCS NO 6 SWIVEL DRIVER
FDA Adverse Event
Malfunction
·TITAN SPINE, LLC·Product code HXX·January 28, 2016
Porex Nostril Retainers, CAT #7241, Size 4, Porex Surgical Inc., 15 Dart Road, Newnan, GA 30265 USA.
FDA Recall
Terminated
·Porex Surgical, Inc.·Product code LYA·July 11, 2006