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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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PrimaLIF LLIF 11mm x 26mm Lordotic Trial
OSTEOMED LLC
817-1011
Not in Commercial Distribution

  • 00845694040785 ()
817-1011

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 9mm x 26mm Lordotic Trial
OSTEOMED LLC
817-1009
Not in Commercial Distribution

  • 00845694040778 ()
817-1009

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 7mm x 26mm Lordotic Trial
OSTEOMED LLC
817-1007
Not in Commercial Distribution

  • 00845694040761 ()
817-1007

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 17mm x 22mm Lordotic Trial
OSTEOMED LLC
816-1017
Not in Commercial Distribution

  • 00845694040754 ()
816-1017

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 15mm x 22mm Lordotic Trial
OSTEOMED LLC
816-1015
Not in Commercial Distribution

  • 00845694040747 ()
816-1015

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 11mm x 22mm Lordotic Trial
OSTEOMED LLC
816-1011
Not in Commercial Distribution

  • 00845694040723 ()
816-1011

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 7mm x 22mm Lordotic Trial
OSTEOMED LLC
816-1007
Not in Commercial Distribution

  • 00845694040709 ()
816-1007

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 15mm x 18mm Lordotic Trial
OSTEOMED LLC
815-1015
Not in Commercial Distribution

  • 00845694040686 ()
815-1015

  • General internal orthopaedic fixation system implantation kit
PrimaLIF LLIF 11mm x 18mm Lordotic Trial
OSTEOMED LLC
815-1011
Not in Commercial Distribution

  • 00845694040662 ()
815-1011

  • General internal orthopaedic fixation system implantation kit
214-0109, Blue ID Tag, CVD BSSO 6H L
OSTEOMED LLC
220-0640-164
In Commercial Distribution

  • 00845694089203 ()
220-0640-164

  • General internal orthopaedic fixation system implantation kit
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