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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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Cup curette, angled DOWN, size “4”
SpineArt SA
SCA-IN 24 01-N
In Commercial Distribution

  • 07640185343344 ()
SCA-IN 24 01-N

  • Bone curette, reusable
Cup curette, straight, size “4”
SpineArt SA
SCA-IN 24 00-N
In Commercial Distribution

  • 07640185343337 ()
SCA-IN 24 00-N

  • Bone curette, reusable
ROD TRIAL LONG
SpineArt SA
ELL-IN 24 02-N
In Commercial Distribution

  • 07640178981829 ()
ELL-IN 24 02-N

  • Spinal implant trial
ROD TRIAL SHORT
SpineArt SA
ELL-IN 24 01-N
In Commercial Distribution

  • 07640178981812 ()
ELL-IN 24 01-N

  • Spinal implant trial
REAMER
SpineArt SA
ELL-IN 24 00-N
In Commercial Distribution

  • 07640178981805 ()
ELL-IN 24 00-N

  • Bone file/rasp, manual, reusable
Reusable Ground Electrode, 32mm Dia Flat Round Disc w/Tip; Green; 1.5mm
IMPULSE MEDICAL TECHNOLOGIES, INC.
EVR-541(24)S
In Commercial Distribution

  • 00816022020298 ()
EVR-541(24)S

  • Analytical non-scalp cutaneous electrode
Sagittal bender left
SpineArt SA
CPF-IN 24 0L-N
Not in Commercial Distribution

  • 07640151095307 ()
CPF-IN 24 0L-N

  • Manual orthopaedic bender, reusable
Sagittal bender right
SpineArt SA
CPF-IN 24 0R-N
Not in Commercial Distribution

  • 07640151095291 ()
CPF-IN 24 0R-N

  • Manual orthopaedic bender, reusable
Sagittal bender left
SpineArt SA
CPF-IN 24 0L-N
In Commercial Distribution

  • 07640178975309 ()
CPF-IN 24 0L-N

  • Manual orthopaedic bender, reusable
Sagittal bender right
SpineArt SA
CPF-IN 24 0R-N
In Commercial Distribution

  • 07640178975293 ()
CPF-IN 24 0R-N

  • Manual orthopaedic bender, reusable
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