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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 7220-1514 TLH 20 DEG 22X14MM
MEDTRONIC SOFAMOR DANEK, INC.
7220-1514
In Commercial Distribution

  • 00191375042396 ()


  • Spinal implant trial
TRIAL 7220-1512 TLH 20 DEG 22X12MM
MEDTRONIC SOFAMOR DANEK, INC.
7220-1512
In Commercial Distribution

  • 00191375042372 ()


  • Spinal implant trial
TBOLT,KWIRE,SS,TROCAR-TROCAR,THRD,20"
Choice Spine, LP
M070-KTS320
In Commercial Distribution

  • 00840996176095 ()


  • Bone-screw internal spinal fixation system, non-sterile
TBOLT,KWIRE,SS,BLUNT-TROCAR,THRD,20"
Choice Spine, LP
M070-KTS220
In Commercial Distribution

  • 00840996176040 ()


  • Bone-screw internal spinal fixation system, non-sterile
TBOLT,KWIRE,SS,BLUNT-BLUNT,THRD,20"
Choice Spine, LP
M070-KTS120
In Commercial Distribution

  • 00840996175999 ()


  • Bone-screw internal spinal fixation system, non-sterile
TBOLT,KWIRE,NIT.,TROCAR-TROCAR,THRD,20"
Choice Spine, LP
M070-KTN320
In Commercial Distribution

  • 00840996175944 ()


  • Bone-screw internal spinal fixation system, non-sterile
TBOLT,KWIRE,NIT.,BLUNT-TROCAR,THRD,20"
Choice Spine, LP
M070-KTN220
In Commercial Distribution

  • 00840996175890 ()


  • Bone-screw internal spinal fixation system, non-sterile
TBOLT,KWIRE,NIT.,BLUNT-BLUNT,THRD,20"
Choice Spine, LP
M070-KTN120
In Commercial Distribution

  • 00840996175845 ()


  • Bone-screw internal spinal fixation system, non-sterile
T'BOLT,KWIRE,SS,TROCAR-TROCAR,LASER,20
Choice Spine, LP
M070-LS320
In Commercial Distribution

  • 00840996173889 ()


  • Spinal guidewire
T'BOLT,KWIRE,SS,BLUNT-TROCAR,LASER,20
Choice Spine, LP
M070-LS220
In Commercial Distribution

  • 00840996173841 ()


  • Spinal guidewire
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