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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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Trial, H 12mm, 20°, L
EIT Emerging Implant Technologies GmbH
AET71240
In Commercial Distribution

  • 04260557774052 ()


  • Spinal implant trial
Hyperlordotic 20°& 25° Spacer Module
Altus Spine, LLC
1020-100H
In Commercial Distribution

  • 00843210186917 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242012T
In Commercial Distribution

  • 00843210182605 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242013T
In Commercial Distribution

  • 00843210182599 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242014T
In Commercial Distribution

  • 00843210182582 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242015T
In Commercial Distribution

  • 00843210182575 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242016T
In Commercial Distribution

  • 00843210182568 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242017T
In Commercial Distribution

  • 00843210182551 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242018T
In Commercial Distribution

  • 00843210182544 ()


  • Polymeric spinal interbody fusion cage
Titanium Interbody, 20 degree, 32mmx24mm
Altus Spine, LLC
SL32242019T
In Commercial Distribution

  • 00843210182537 ()


  • Polymeric spinal interbody fusion cage
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