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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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114-2015, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-83
In Commercial Distribution

  • 00845694088749 ()
220-0643-83

  • General internal orthopaedic fixation system implantation kit
220-0565, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-82
In Commercial Distribution

  • 00845694088732 ()
220-0643-82

  • General internal orthopaedic fixation system implantation kit
220-0561, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-80
In Commercial Distribution

  • 00845694088725 ()
220-0643-80

  • General internal orthopaedic fixation system implantation kit
220-0324, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-78
In Commercial Distribution

  • 00845694088718 ()
220-0643-78

  • General internal orthopaedic fixation system implantation kit
220-0007, Purple ID Tag, 1.6 MANUAL
OSTEOMED LLC
220-0643-48
In Commercial Distribution

  • 00845694088541 ()
220-0643-48

  • General internal orthopaedic fixation system implantation kit
220-0004, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-45
In Commercial Distribution

  • 00845694088534 ()
220-0643-45

  • General internal orthopaedic fixation system implantation kit
220-0003, Purple ID Tag, Angled Locking
OSTEOMED LLC
220-0643-44
In Commercial Distribution

  • 00845694088527 ()
220-0643-44

  • General internal orthopaedic fixation system implantation kit
220-0121, Blue ID Tag, 2.0/2.4DL
OSTEOMED LLC
220-0640-143
In Commercial Distribution

  • 00845694088503 ()
220-0640-143

  • General internal orthopaedic fixation system implantation kit
212-0136 White ID Tag, EXT X
OSTEOMED LLC
220-0641-25
In Commercial Distribution

  • 00845694058254 ()
220-0641-25

  • General internal orthopaedic fixation system implantation kit
212-0086 White ID Tag, ORBITAL LRG
OSTEOMED LLC
220-0641-21
In Commercial Distribution

  • 00845694058216 ()
220-0641-21

  • General internal orthopaedic fixation system implantation kit
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