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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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220-0013, Blue ID Tag, 1.6 4MM ST J
OSTEOMED LLC
220-0640-135
In Commercial Distribution

  • 00845694061339 ()
220-0640-135

  • General internal orthopaedic fixation system implantation kit
220-0012, Blue ID Tag, 1.6 6MM STP J
OSTEOMED LLC
220-0640-134
In Commercial Distribution

  • 00845694061322 ()
220-0640-134

  • General internal orthopaedic fixation system implantation kit
220-0007, Blue ID Tag, 1.6 MANUAL
OSTEOMED LLC
220-0640-133
In Commercial Distribution

  • 00845694061315 ()
220-0640-133

  • General internal orthopaedic fixation system implantation kit
220-0004, Blue ID Tag, 1.6 LONG JL
OSTEOMED LLC
220-0640-132
In Commercial Distribution

  • 00845694061308 ()
220-0640-132

  • General internal orthopaedic fixation system implantation kit
220-0003, Blue ID Tag, 1.6 JL
OSTEOMED LLC
220-0640-131
In Commercial Distribution

  • 00845694061292 ()
220-0640-131

  • General internal orthopaedic fixation system implantation kit
212-1694, White ID Tag, ORB PREF R.5
OSTEOMED LLC
220-0641-73
In Commercial Distribution

  • 00845694061285 ()
220-0641-73

  • General internal orthopaedic fixation system implantation kit
212-1693, White ID Tag, ORB PREF R.4
OSTEOMED LLC
220-0641-72
In Commercial Distribution

  • 00845694061278 ()
220-0641-72

  • General internal orthopaedic fixation system implantation kit
212-1692, White ID Tag, ORB PREF R.3
OSTEOMED LLC
220-0641-71
In Commercial Distribution

  • 00845694061261 ()
220-0641-71

  • General internal orthopaedic fixation system implantation kit
212-1691, White ID Tag, ORB PREF R.2
OSTEOMED LLC
220-0641-70
In Commercial Distribution

  • 00845694061254 ()
220-0641-70

  • General internal orthopaedic fixation system implantation kit
212-1684, White ID Tag, ORB PREF L.5
OSTEOMED LLC
220-0641-69
In Commercial Distribution

  • 00845694061247 ()
220-0641-69

  • General internal orthopaedic fixation system implantation kit
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