21 results
·
21ms
·
Sources: EU EUDAMED, US FDA
PEDIATRIC IV WATCH
FDA 510(k)
FDA Class 2
·General Hospital
CoRoent
FDA UDI
Nuvasive, Inc.·00887517380715·CoRoent Contoured Trial, 10L
LEONE SPA
FDA UDI
LEONE SPA·08033707030768·WEB 1ST MOL BANDS W/G8325-02 UR 30
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057632·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057700·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057670·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057663·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057717·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057625·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057649·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057656·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057687·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057724·
FRS™CANNULATED SCREW
FDA UDI
Biomet Orthopedics, LLC·00887868057694·
SURGEON'S GLOVE, POWDER FREE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Hisense 2MP/3MP LCD Monitor (HMD2C21/HMD3C21)
FDA 510(k)
FDA Class 2
·Radiology
ADVIA LABCELL
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 5, 2014
UNKNOWN DEPUY ASR ACETABULAR CUP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·November 30, 2012
2600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 28, 2010
BIOMET StageOne Knee Tibial Cement Spacer Mold, 70 MM, Silicone, Sterile, Item 433170.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020