10,000 results
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741ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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INW Server
FDA UDI
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.·00840682123563·SOFTWARE INW SERVER V6.9.6 R3
INW Server
FDA UDI
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC.·00840682145756·Software Medical Device INW V7.0
HEEL/ELBOW PROTECTOR
FDA Adverse Event
MEDLINE INDUSTRIES, INC.·Product code FMP·January 18, 1995
MEDTRONIC
FDA Adverse Event
Injury
·MEDTRONIC·Product code LWS·August 9, 2006
COBLATION
FDA Adverse Event
Malfunction
·SMITH & NEPHEW, INC.·Product code GEI·June 21, 2023
microAIR MA800 42 in W x 84 in L Mattress
FDA UDI
INVACARE CORPORATION·00841447103219·microAIR MA800 42"W x 84"L Mattress
VANDER LIFT II
FDA Adverse Event
Injury
·VANCARE, INC.·Product code FSA·May 20, 2013
GYNECARE MORCELLEX
FDA Adverse Event
ETHICON, INC.·Product code HET·October 23, 2012
CHAIR CHECK DEVICE
FDA Adverse Event
Other
·BED-CHECK CORP.·Product code KMI·December 4, 1996
UNK
FDA Adverse Event
UNK·Product code IOR·June 29, 2006
LIGACLIP MCA MED LONG APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDO·February 10, 2017
LABAC
FDA Adverse Event
Injury
·UNK·Product code IOR·May 21, 1999
2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 24, 2009
5385024
FDA Adverse Event
Malfunction
·January 22, 2016
LOCKING PEG, T7, DIAM.2.0X20MM
FDA Adverse Event
Malfunction
·STRYKER LEIBINGER FREIBURG·Product code HRS·June 26, 2017
BD SEDITAINER¿ 0.105M 1.25ML BUFFERED SODIUM CITRATE BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 22, 2019
INSERTION HANDLE F/TROCHANTERIC FIXATION NAILS
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code JDS·August 16, 2011
CLOSED SYSTEM TRANSFER DEVICE PHASEAL PROTECTOR
FDA Adverse Event
Other
·BECTON DICKINSON·Product code ONB·July 17, 2025
CLOSED SYSTEM TRANSFER DEVICE PHASEAL PROTECTOR
FDA Adverse Event
Other
·BECTON DICKINSON·Product code ONB·July 17, 2025
WOUNDSTAT HEMOSTATIC AGENT
FDA Adverse Event
Malfunction
·TRAUMACURE, INC.·Product code LMF·July 22, 2009