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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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LTX SPACER, 6 x 18 x 45 mm, 20°
ALPHATEC SPINE, INC.
261-06184520
In Commercial Distribution

  • 00190376522661 ()


  • Polymeric spinal interbody fusion cage
LTX TRIAL, 6 x 22 x 60 mm, 20°
ALPHATEC SPINE, INC.
262-06226020
In Commercial Distribution

  • 00190376522050 ()


  • Spinal implant trial
LTX SPACER, 6 x 22 x 45 mm, 20°
ALPHATEC SPINE, INC.
261-06224520
In Commercial Distribution

  • 00190376522838 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 22 x 60 mm, 20°
ALPHATEC SPINE, INC.
261-06226020
In Commercial Distribution

  • 00190376522531 ()


  • Polymeric spinal interbody fusion cage
LTX SPACER, 6 x 22 x 55 mm, 20°
ALPHATEC SPINE, INC.
261-06225520
In Commercial Distribution

  • 00190376522494 ()


  • Polymeric spinal interbody fusion cage
LTX TRIAL, 6 x 18 x 60 mm, 20°
ALPHATEC SPINE, INC.
262-06186020
In Commercial Distribution

  • 00190376522036 ()


  • Spinal implant trial
Cervical Left Side Rod to Rod Connector Ø4.6x11.3x15.0mm, 20°
Aegis Spine, Inc.
6142-3248
In Commercial Distribution

  • 00840273310556 ()
6142-3248

  • Bone-screw internal spinal fixation system, non-sterile
Cervical Left Side Rod to Rod Connector 11.3x16.5mm, 20°
Aegis Spine, Inc.
6142-3230
In Commercial Distribution

  • 00840273310457 ()
6142-3230

  • Bone-screw internal spinal fixation system, non-sterile
Cervical Left Side Rod to Rod Connector 11.3x15.5mm, 20°
Aegis Spine, Inc.
6142-3239
In Commercial Distribution

  • 00840273310440 ()
6142-3239

  • Bone-screw internal spinal fixation system, non-sterile
Cervical Right Side Rod to Rod Connector Ø6.1x12.8x18.5mm, 20°
Aegis Spine, Inc.
6142-2260
In Commercial Distribution

  • 00840273310396 ()
6142-2260

  • Bone-screw internal spinal fixation system, non-sterile
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