2,623 results
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49ms
·
Sources: EU EUDAMED, US FDA
Portex
FDA UDI
Smiths Medical International Ltd·15019315103414·
Portex
FDA UDI
Smiths Medical International Ltd·15019315076770·
Portex
FDA UDI
Smiths Medical International Ltd·10351688409850·
Portex
FDA UDI
Smiths Medical International Ltd·15019315079849·
Portex
FDA UDI
Smiths Medical International Ltd·15019315060168·
Portex
FDA UDI
Smiths Medical International Ltd·10351688433831·
InHealth Technologies; Blom-Singer
FDA UDI
Freudenberg Medical, LLC·00848253003429·Post-Operative Care Kit with 10/55 Tube & EasyF...
Portex
FDA UDI
Smiths Medical International Ltd·15019315096303·
Portex
FDA UDI
Smiths Medical International Ltd·10351688414540·
BE SMART GET PREPARED
FDA UDI
TOTAL RESOURCES INTERNATIONAL INC.·00020424101138·OSHA / ANSI First Aid Kit, 50-Person, 250 Piece...
BE SMART GET PREPARED
FDA UDI
TOTAL RESOURCES INTERNATIONAL INC.·00020424050030·OSHA / ANSI First Aid Kit – 251 pcs - (2) Silve...
BE SMART GET PREPARED
FDA UDI
TOTAL RESOURCES INTERNATIONAL INC.·00020424011130·OSHA / ANSI First Aid Kit, 50-Person, 250 Piece...
BE SMART GET PREPARED
FDA UDI
TOTAL RESOURCES INTERNATIONAL INC.·00020424013493·OSHA / ANSI First Aid Kit, 50-Person, 251 Piece...
BE SMART GET PREPARED
FDA UDI
TOTAL RESOURCES INTERNATIONAL INC.·00020424011727·OSHA / ANSI First Aid Kit, 50-Person, 256 Piece...
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·VISTA LORDOTIC INTERBODY FUSION CAGE
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VITALITY AVT AND THE PROGRAMMER SOFTWARE APPLICATION MODEL 2812
Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction
FDA Pre-Market Approval
FDA Class 3
·INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA Pre-Market Approval
FDA Class 2
·BAK INTERBODY FUSION SYSTEM, BP/LORDOTIC DEVICE
Separator, Automated, Blood Cell And Plasma, Therapeutic
FDA Pre-Market Approval
FDA Unclassified
·PROSORBA COLUMN
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK VITALITY AVT AICD, MODELS A135 AND A155, MODEL 2920 PROGRAMMER WITH MODEL 2812 APPLICATION SOFTWARE VERSION 1.2