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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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Screw-Screw Distractor - C-C, Integrated Set Screw - Right
ALPHATEC SPINE, INC.
CI-10238-100
In Commercial Distribution

  • 00811801035128 ()


  • Orthopaedic surgical distractor, internal
MaXcess MAS TLIF Blade, 120mm C-C Tube
Nuvasive, Inc.
1628289
In Commercial Distribution

  • 00887517146120 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 110mm C-C Tube
Nuvasive, Inc.
1628288
In Commercial Distribution

  • 00887517146113 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 100mm C-C Tube
Nuvasive, Inc.
1628287
In Commercial Distribution

  • 00887517146106 ()


  • Surgical retraction system, reusable
Camber Trad Plate, 14mm Lg Lamina C-C
Nuvasive, Inc.
8370020P
In Commercial Distribution

  • 00887517995773 ()


  • Spinal fixation plate, non-bioabsorbable
Camber Trad Plate, 10mm Lg Lamina C-C
Nuvasive, Inc.
8370018P
In Commercial Distribution

  • 00887517995759 ()


  • Spinal fixation plate, non-bioabsorbable
MaXcess MAS TLIF Blade, 100mm Right C-C
Nuvasive, Inc.
1685307
In Commercial Distribution

  • 00887517614469 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 90mm Right C-C
Nuvasive, Inc.
1685306
In Commercial Distribution

  • 00887517614452 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 80mm Right C-C
Nuvasive, Inc.
1685305
In Commercial Distribution

  • 00887517614445 ()


  • Surgical retraction system, reusable
MaXcess MAS TLIF Blade, 70mm Right C-C
Nuvasive, Inc.
1685304
In Commercial Distribution

  • 00887517614438 ()


  • Surgical retraction system, reusable
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