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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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Over Baseplate Reamer 45/24
ARTHREX, INC.
AR-9632-2445
In Commercial Distribution

  • 00888867308183 ()
AR-9632-2445

  • Bone-resection orthopaedic reamer, reusable
Speed Guide, Nonlocking Screw 24
ARTHREX, INC.
AR-9630-24NL
In Commercial Distribution

  • 00888867298590 ()
AR-9630-24NL

  • Joint prosthesis implantation kit, reusable
R438 Molt 2-4 Surgical Curette
PDT, INC.
R438 Molt 2-4 Surgical Curette
In Commercial Distribution

  • 00813677024589 ()
R438

  • General-purpose curette
ALIF Bone Packing Block 24
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809263397832 ()
SCAI-026

  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,SS,TROCAR-TROCAR,24"
Choice Spine, LP
M070-KS324
In Commercial Distribution

  • 00840996135818 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,SS,BLUNT-TROCAR,24"
Choice Spine, LP
M070-KS224
In Commercial Distribution

  • 00840996135771 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,SS,BLUNT-BLUNT,24"
Choice Spine, LP
M070-KS124
In Commercial Distribution

  • 00840996135733 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,NITL,TROCAR-TROCAR,24"
Choice Spine, LP
M070-KN324
In Commercial Distribution

  • 00840996135696 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,NITOL,BLUNT-TROCAR,24"
Choice Spine, LP
M070-KN224
In Commercial Distribution

  • 00840996135658 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,NITOL,BLUNT-BLUNT,24"
Choice Spine, LP
M070-KN124
In Commercial Distribution

  • 00840996135610 ()


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