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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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220-0067, Gray ID Tag, 1.6 STEM DL
OSTEOMED LLC
220-0644-62
In Commercial Distribution

  • 00845694060486 ()
220-0644-62

  • General internal orthopaedic fixation system implantation kit
220-0062, Gray ID Tag, 1.3 16STP JL
OSTEOMED LLC
220-0644-59
In Commercial Distribution

  • 00845694060455 ()
220-0644-59

  • General internal orthopaedic fixation system implantation kit
220-0899, Purple ID Tag, 2.0 RAINBW JL
OSTEOMED LLC
220-0643-90
In Commercial Distribution

  • 00845694060257 ()
220-0643-90

  • General internal orthopaedic fixation system implantation kit
220-0560, Purple ID Tag, 2.0 EXT JL
OSTEOMED LLC
220-0643-79
In Commercial Distribution

  • 00845694060240 ()
220-0643-79

  • General internal orthopaedic fixation system implantation kit
220-0006, Purple ID Tag, 2.0PD EXT J
OSTEOMED LLC
220-0643-47
In Commercial Distribution

  • 00845694060233 ()
220-0643-47

  • General internal orthopaedic fixation system implantation kit
220-0005, Purple ID Tag, 2.0 12STP JL
OSTEOMED LLC
220-0643-46
In Commercial Distribution

  • 00845694060226 ()
220-0643-46

  • General internal orthopaedic fixation system implantation kit
231-2814, Purple ID Tag, RCN 5X16 RT
OSTEOMED LLC
220-0643-41
In Commercial Distribution

  • 00845694060196 ()
220-0643-41

  • General internal orthopaedic fixation system implantation kit
231-2813, Purple ID Tag, RCN 5X16 LT
OSTEOMED LLC
220-0643-40
In Commercial Distribution

  • 00845694060189 ()
220-0643-40

  • General internal orthopaedic fixation system implantation kit
231-2812, Purple ID Tag, RCN 4X12 RT
OSTEOMED LLC
220-0643-39
In Commercial Distribution

  • 00845694060172 ()
220-0643-39

  • General internal orthopaedic fixation system implantation kit
231-2811, Purple ID Tag, RCN 4X12 LT
OSTEOMED LLC
220-0643-38
In Commercial Distribution

  • 00845694060165 ()
220-0643-38

  • General internal orthopaedic fixation system implantation kit
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