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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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LF2 W/PYR 24 L 3/8 236-300#
TRULIFE LIMITED
SLF195-24-L-H9
In Commercial Distribution

  • 00645517576763 ()


  • Mechanical-resistance external ankle-foot prosthesis
LF2 W/PYR 24 L 3/8 185-235#
TRULIFE LIMITED
SLF195-24-L-H8
In Commercial Distribution

  • 00645517576756 ()


  • Mechanical-resistance external ankle-foot prosthesis
LF2 W/PYR 24 L 3/8 145-184#
TRULIFE LIMITED
SLF195-24-L-H7
In Commercial Distribution

  • 00645517576749 ()


  • Mechanical-resistance external ankle-foot prosthesis
LF2 W/PYR 24 L 3/8 114-144#
TRULIFE LIMITED
SLF195-24-L-H6
In Commercial Distribution

  • 00645517576732 ()


  • Mechanical-resistance external ankle-foot prosthesis
LF2 W/PYR 24 L 3/8 90-113#
TRULIFE LIMITED
SLF195-24-L-H5
In Commercial Distribution

  • 00645517576725 ()


  • Mechanical-resistance external ankle-foot prosthesis
Insert Aluminum (L)24 (W)12 (H)2
K1 MEDICAL TECHNOLOGIES, LLC
137 INSERT.AL.24.12.2
In Commercial Distribution

  • 00850025473705 ()
137 INSERT.AL.24.12.2

  • Instrument tray, reusable
Insert Aluminum (L)24 (W)12 (H)2
K1 MEDICAL TECHNOLOGIES, LLC
060 INSERT.AL.24.12.2
In Commercial Distribution

  • 00850025473101 ()
060 INSERT.AL.24.12.2

  • Instrument tray, reusable
Foot Kinetic Light, No Pylon RT 24 #4
TRULIFE LIMITED
SKF110-24-R-4B4
In Commercial Distribution

  • 00645517893921 ()


  • Mechanical-resistance external ankle-foot prosthesis
Foot Kinetic Light, No Pylon RT 24 #2
TRULIFE LIMITED
SKF110-24-R-2A4
In Commercial Distribution

  • 00645517893907 ()


  • Mechanical-resistance external ankle-foot prosthesis
Foot Kinetic Light, No Pylon LFT 24 #3
TRULIFE LIMITED
0800502
In Commercial Distribution

  • 00645517893884 ()


  • Mechanical-resistance external ankle-foot prosthesis
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