10,000 results · 108ms · Sources: EU EUDAMED, US FDA

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FDA UDI
ALPHATEC SPINE, INC.·00190376522777·LTX DOMED SPACER, 6 x 18 x 60 mm, 15°

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FDA UDI
ALPHATEC SPINE, INC.·00190376522678·LTX DOMED SPACER, 6 x 18 x 45 mm, 20°

LIFE LINER

FDA UDI
DEPUY ORTHOPAEDICS, INC.·10603295326373·LIFE LINER STICK & CUT REST GLV LT X-LG

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FDA UDI
ALPHATEC SPINE, INC.·00190376473949·LTX HL SPACER, 6 x 22 x 50 mm, 30°

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FDA UDI
ALPHATEC SPINE, INC.·00190376522807·LTX DOMED SPACER, 6 x 18 x 60 mm, 20°

Ontrak

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522129230·CUFF,ABP,ADULT M,24-32CM/9-13IN,NO LTX

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FDA UDI
ALPHATEC SPINE, INC.·00190376522715·LTX DOMED SPACER, 6 x 18 x 50 mm, 20°

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FDA UDI
ALPHATEC SPINE, INC.·00190376474007·LTX HL SPACER, 6 x 22 x 60 mm, 30°

Ontrak

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522129254·CUFF,ABP,ADULT,L,32-42CM/13-17IN,NO LTX

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FDA UDI
ALPHATEC SPINE, INC.·00190376473970·LTX HL SPACER, 6 x 22 x 55 mm, 30°

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FDA UDI
ALPHATEC SPINE, INC.·00190376522739·LTX DOMED SPACER, 6 x 18 x 55 mm, 15°

OnTrak

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102547·CUFF,ABP,XLGADLT,38-50CM/15-20IN,NO LTX,QKD/LEUR

FOGARTY SAFEJAW

FDA UDI
Edwards Lifesciences LLC·00690103043914·SPRING CLIP,DBL SAFEJAW 6MM FOGARTY,LTX FREE,ST...

OnTrak

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102530·CUFF,ABP,LG ADLT,32-42CM/13-17IN,NO LTX,QKD/LUER

OnTrak

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102233·CUFF,ABP,SM ADLT,17-26CM/7-10IN,NO LTX,QKD/LUER

OnTrak

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102240·CUFF,ABP,ADLT,24-32CM/9-13IN,NO LTX,QK DISC/LUER

ACU-EVAC

FDA UDI
ACUDERM, INC.·00814105020524·Hose connector used to connect TX Pack or LTX P...

OnTrak

FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102257·CUFF,ABP,CHILD,12-20CM/5-8IN,NO LTX,QK DISC/LUER

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·Intellis Spinal Cord Stimulation Systems

Implanted Electrical Device Intended For Treatment Of Fecal Incontinence

FDA Pre-Market Approval
FDA Class 3 ·InterStim® Therapy System, Verify® Evaluation System