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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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F3D Lateral 18mm x 45mm x 16mm x 20°
CORELINK LLC
3LL1845-2016
In Commercial Distribution

  • M7253LL18452016 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 18mm x 45mm x 14mm x 20°
CORELINK LLC
3LL1845-2014
In Commercial Distribution

  • M7253LL18452014 ()


  • Spinal fixation plate, non-bioabsorbable
F3D Lateral 18mm x 45mm x 12mm x 20°
CORELINK LLC
3LL1845-2012
In Commercial Distribution

  • M7253LL18452012 ()


  • Spinal fixation plate, non-bioabsorbable
Trial Rasp, 39mm x 30mm x 18mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-231820
In Commercial Distribution

  • 10889981309992 ()
RA2-231820

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 16mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-231620
In Commercial Distribution

  • 10889981309985 ()
RA2-231620

  • Bone file/rasp, manual, reusable
Trial Rasp, 39mm x 30mm x 14mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-231420
In Commercial Distribution

  • 10889981309954 ()
RA2-231420

  • Bone file/rasp, manual, reusable
Trial Rasp, 35mm x 27mm x 18mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-211820
In Commercial Distribution

  • 10889981309886 ()
RA2-211820

  • Bone file/rasp, manual, reusable
Trial Rasp, 35mm x 27mm x 16mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-211620
In Commercial Distribution

  • 10889981309879 ()
RA2-211620

  • Bone file/rasp, manual, reusable
Trial Rasp, 35mm x 27mm x 14mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-211420
In Commercial Distribution

  • 10889981309848 ()
RA2-211420

  • Bone file/rasp, manual, reusable
Trial Rasp, 31mm x 24mm x 18mm, 20 Deg
Seaspine Orthopedics Corporation
RA2-201820
In Commercial Distribution

  • 10889981309763 ()
RA2-201820

  • Bone file/rasp, manual, reusable
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