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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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STATION,PATIENT,CC/PS,JERON,SINGLE
Crest Healthcare Supply
6420C
In Commercial Distribution

  • B4846420C0 ()


  • Nurse call system
Bone Graft Delivery System, 30 cc
SPINEEX, INC.
013-030-11
In Commercial Distribution

  • 00819837021221 ()

  • Total Volume: 30 Milliliter
013-030-11

  • Bone graft funnel
Toomey Evacuator 50 cc With Adapter
Gyrus ACMI, LLC
188A
In Commercial Distribution

  • 00821925001077 ()


  • Bladder evacuator, reusable
Toomey Evacuator 30 cc, With Adapter
Gyrus ACMI, LLC
188
In Commercial Distribution

  • 00821925001053 ()


  • Bladder evacuator, reusable
ID II LIF Inserter Sleeve, C-C
ALPHATEC SPINE, INC.
801-140-50
In Commercial Distribution

  • 00190376635439 ()


  • Orthopaedic inorganic implant inserter/extractor, reusable
AlloFuse® DBM Gel, 5 cc
ALLOSOURCE
90138005
In Commercial Distribution

  • M536901380051 ()

  • 5 cc
90138005

  • Bone matrix implant, human-derived
AlloFuse® DBM Gel, 1 cc
ALLOSOURCE
90138001
In Commercial Distribution

  • M536901380011 ()

  • 1 cc
90138001

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 10 cc
ALLOSOURCE
90038010
In Commercial Distribution

  • M536900380101 ()

  • 10 cc
90038010

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 5 cc
ALLOSOURCE
90038005
In Commercial Distribution

  • M536900380051 ()

  • 5 cc
90038005

  • Bone matrix implant, human-derived
AlloFuse® DBM Putty, 2.5 cc
ALLOSOURCE
90038002
In Commercial Distribution

  • M536900380021 ()

  • 2.5 cc
90038002

  • Bone matrix implant, human-derived
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