29 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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mCare® Powder Free Nitrile Black Examination Glove
FDA 510(k)
FDA Class 1
·General Hospital
OsteoMed
FDA UDI
OSTEOMED LLC·00845694015516·2.4mm x 44mm Cannulated Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070966·Cannulated 2.4 x 44mm Lag Screw Sterile Qty 2
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
ANATOMIC PEEK CERVICAL FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
TACTICATH
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code OAE·January 11, 2016
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·August 6, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·October 17, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·November 9, 2018
ROSA ONE
FDA Adverse Event
Injury
·MEDTECH SA·Product code HAW·January 11, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code NAY·January 21, 2019
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code HAW·December 21, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018
BARD WOUND DRAIN
FDA Adverse Event
Injury
·C.R. BARD, INC.·Product code GBX·October 7, 2008
NORMALLY CLOSED CHECK VALVE/ANTISIPHON VALVE
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL, INC.·Product code FPA·June 19, 2013
AP LRG W/RAPIDPORT EZ
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·July 26, 2011
ROSA ONE
FDA Adverse Event
Malfunction
·MEDTECH SA·Product code OLO·November 15, 2018