69 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PAINFUSOR CATHETER
FDA 510(k)
FDA Class 2
·Anesthesiology
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR31110311·Titanol instant tension springs 18 mm light
Sklar
FDA UDI
SKLAR CORPORATION·10649111457579·EISELSBERG LIG SCISS CVD 4.25 IN
Surgical Instrument
FDA UDI
Jeil Medical Corporation·08809265158868·
MicroSelectron Digital
FDA UDI
Nucletron B.V.·08717213015142·microSelectron Transfer Tube Set for 6F Flexibl...
VYSIS UROVYSION BLADDER CANCER RECURRENCE KIT
FDA 510(k)
FDA Class 2
·Immunology
MASIMO DISPOSABLE OXIMETRY EAR SENSOR, MODEL E1
FDA 510(k)
FDA Class 2
·Cardiovascular
BD PLASTIPAK¿ CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·May 16, 2022
BD PLASTIPAK¿ CONCENTRIC LUER LOCK SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·February 15, 2022
UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT
FDA Adverse Event
Malfunction
·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022
MAQUET SAS
FDA Adverse Event
Malfunction
·MAQUET S.A.·Product code FSY·April 8, 2013
GMK FEMORAL CUTTING GUIDE
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·April 13, 2011
PUREVISION TORIC (BALAFILCON A) CONTACT LENS
FDA Adverse Event
Injury
·BAUSCH & LOMB·Product code LPM·August 12, 2008
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code HWC·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 40
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 45
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 35
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019
TL PEDICLE SCREW DIA. 6,5 LG 50
FDA Adverse Event
Malfunction
·ZIMMER SPINE·Product code NKB·July 9, 2019