986 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA UDI
Drive Devilbiss Healthcare·00822383586373·RespiratoryNebs Product Description: PowerNeb,w...
TraumaOne SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00888233021210·
FMT
FDA UDI
METKO MEDIKAL VE TIBBI CIHAZLAR DIS TICARET LIMITED SIRKETI·08698870376404·Temperature Probe Adapter and Extension Cable
TRAUMAONE SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036168216·
TraumaOne SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00888233021272·
TRAUMAONE SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036165475·
TRAUMAONE SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036168193·
TraumaOne SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00888233021258·
GE OEC 2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 3, 2008
NEOTECH
FDA Adverse Event
Malfunction
·NEOTECH·Product code FOK·December 6, 2016
HUT EXT DR FINAL ASSY-REVERSE
FDA Adverse Event
Malfunction
·LIEBEL-FLARSHEIM·Product code IXR·January 11, 2019
Philips Medical System Allura Xper X-Ray Angiographic
FDA Enforcement
Class II
·Terminated·Philips Medical Systems, Inc.·March 11, 2015
UNKN SUSPENSORY FIXATION DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·July 11, 2023
UNKN SUSPENSORY FIXATION DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·July 11, 2023
UNKN SUSPENSORY FIXATION DEV
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MBI·July 11, 2023
UNK KNEE TIBIAL TRAY SIGMA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code NJL·August 19, 2021
UNK KNEE FEMORAL SIGMA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code NJL·August 19, 2021
UNK KNEE TIBIAL INSERT SIGMA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code NJL·August 19, 2021
GE Healthcare Definium 8000 Digital Radiographic System, model number 5135678. GE Healthcare, 3000 North Grandview, Waukesha, WI 53188 U.S.A. The intended use of this product is to generate tomographic images of human anatomy.
FDA Recall
Terminated
·GE Healthcare·Product code KPR·January 2, 2008
Precision 500D Classical R&F System with control room PC; Image-intensified fluoroscopic x-ray system; ; Model Number: 5117866-27.
FDA Recall
Terminated
·GE Healthcare·Product code JAA·August 1, 2007