17 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEWLETT-PACKARD MODEL M1018A TCPO2/TOPCO2 MODULE
FDA 510(k)
FDA Class 2
·Anesthesiology
Lode B.V.
FDA UDI
Lode B.V.·08717524640224·925910 Brachumera Sport PFM
OXYGEN POWERED RESUSCITATOR FOR CPR
FDA 510(k)
FDA Class 2
·Anesthesiology
STERRAD CHEMICAL INDICATOR
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
STERILMED, INC.·10888551007580·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007573·SAW BLADE SAGITTAL FLARED K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007559·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007566·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007603·SAW BLADE SAGITTAL K9 K2000 SERIES
NA
FDA UDI
STERILMED, INC.·10888551007597·SAW BLADE SAGITTAL K9 K2000 SERIES
DRILL BIT Ø1.1 W/STOP L44.5/8 2FLUTE
FDA Adverse Event
Malfunction
·SYNTHES·Product code HSZ·January 22, 2013
ENDO STITCH SURGIDAC 2/0 48 GRN DLU SU
FDA Adverse Event
Malfunction
·UNITED STATES SURGICAL·Product code KOG·November 23, 2010
OPTISENSE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·July 10, 2014
ENDOLOOP LIGATURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GEA·December 27, 2018
CER BIOLOXD MOD HD 36MM -3 NK
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·April 28, 2020
G7 NEUTRAL E1 LINER 36MM F
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·April 13, 2020
G7 PPS LTD ACET SHELL 54F
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·April 13, 2020