27 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SMARTLUX
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Head rest Breast BI
FDA UDI
Noras MRI products GmbH·04251269206962·The intended use of Breast BI Coil Set 0.55T is...
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529585556·Apex Femoral Nail PF Right Ø 12.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529586454·Apex Femoral Nail GT Left Ø 12.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529588335·Apex Femoral Nail Retrograde Ø 12.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529583217·Apex Femoral Nail PF Left Ø 12.0 x 460mm
Apex
FDA UDI
ORTHOXEL DESIGNATED ACTIVITY COMPANY·05391529587352·Apex Femoral Nail GT Right Ø 12.0 x 460mm
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450193501·
Logical Cup Liner
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215054212·
AED
FDA UDI
NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657017800·90 degree Punch blunt 3.5mm right angled
Logical 20° Hooded Liner
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215009472·
AMBIT INTRODUCER, AMBIT NEEDLE, AMBIT SHEATH
FDA 510(k)
FDA Class 2
·Anesthesiology
E-CUBE 9
FDA 510(k)
FDA Class 2
·Radiology
OrthoMedFlex
FDA UDI
ORTHOMEDFLEX LLC·M7161111204600·Liner, 40-60/68mm (20° Hood)
VENTO XLPE Liner
FDA UDI
AMPLITUDE SAS·03701089514644·
OXF ANAT BRG RT SM SIZE 3 PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·December 19, 2023
OXF TWIN-PEG CMNTD FEM SM PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·December 19, 2023
TOTAL ASR FEM IMP SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2014
INTERNATIONAL INFINITY ENTERAL FEEDING PUMP
FDA Adverse Event
Other
·MOOG MEDICAL DEVICES GROUP·Product code LZH·May 25, 2011