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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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PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242018
In Commercial Distribution

  • 00843210159720 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242017
In Commercial Distribution

  • 00843210159713 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242016
In Commercial Distribution

  • 00843210159706 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242015
In Commercial Distribution

  • 00843210159690 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242014
In Commercial Distribution

  • 00843210159683 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242013
In Commercial Distribution

  • 00843210159676 ()


  • Polymeric spinal interbody fusion cage
PEEK/Titanium Interbody, 20 °, 32mm x 24mm
Altus Spine, LLC
SL32242012
In Commercial Distribution

  • 00843210159669 ()


  • Polymeric spinal interbody fusion cage
Cannulated screw 4.5, L 20, full thread
aap Implantate AG
445320
Not in Commercial Distribution

  • EATO4453209 ()
445320

  • Orthopaedic bone screw (non-sliding)
Cannulated screw 4.0, L 20, full thread
aap Implantate AG
440320
Not in Commercial Distribution

  • EATO4403209 ()
440320

  • Orthopaedic bone screw (non-sliding)
POL GN BR 2-0 KT-2 2N 30
TELEFLEX INCORPORATED
IPN009424
In Commercial Distribution

  • 44026704420405 ()
  • 24026704420401 ()
  • 04026704420407 ()

  • 'silky' II POLYDEK® /Needle KT-2, KT-2 Size-2-0
  • Length: 75 Centimeter
69-717

  • Polyester suture, non-bioabsorbable, multifilament
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