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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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POST NAV ROTATING DISTRACTOR, 11mm
ALPHATEC SPINE, INC.
244-03-000-11-N
In Commercial Distribution

  • 00190376529264 ()

  • Width: 11 Millimeter


  • Bone lever/elevator, reusable
POST NAV ROTATING DISTRACTOR, 10mm
ALPHATEC SPINE, INC.
244-03-000-10-N
In Commercial Distribution

  • 00190376529257 ()

  • Width: 10 Millimeter


  • Bone lever/elevator, reusable
POST NAV ROTATING DISTRACTOR, 9mm
ALPHATEC SPINE, INC.
244-03-000-09-N
In Commercial Distribution

  • 00190376529240 ()

  • Width: 9 Millimeter


  • Bone lever/elevator, reusable
POST NAV ROTATING DISTRACTOR, 8mm
ALPHATEC SPINE, INC.
244-03-000-08-N
In Commercial Distribution

  • 00190376529233 ()

  • Width: 8 Millimeter


  • Bone lever/elevator, reusable
POST NAV ROTATING DISTRACTOR, 7mm
ALPHATEC SPINE, INC.
244-03-000-07-N
In Commercial Distribution

  • 00190376529226 ()

  • Width: 7 Millimeter


  • Bone lever/elevator, reusable
POST NAV ROTATING DISTRACTOR, 6mm
ALPHATEC SPINE, INC.
244-03-000-06-N
In Commercial Distribution

  • 00190376529219 ()

  • Width: 6 Millimeter


  • Bone lever/elevator, reusable
POST NAV RIGHT-BEND CUP CURETTE, SIZE 2
ALPHATEC SPINE, INC.
244-14-400-02-N
In Commercial Distribution

  • 00190376529042 ()


  • Bone curette, reusable
POST NAV LEFT-BEND CUP CURETTE, SIZE 2
ALPHATEC SPINE, INC.
244-14-300-02-N
In Commercial Distribution

  • 00190376529035 ()


  • Bone curette, reusable
POST NAV PUSH CUP CURETTE, SIZE 2
ALPHATEC SPINE, INC.
244-14-020-02-N
In Commercial Distribution

  • 00190376529028 ()


  • Bone curette, reusable
POST NAV STRAIGHT CUP CURETTE, SIZE 2
ALPHATEC SPINE, INC.
244-14-000-02-N
In Commercial Distribution

  • 00190376529004 ()


  • Bone curette, reusable
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