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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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39 +2.5 INF/24 Glenosphere
ARTHREX, INC.
AR-9564-2439-INF
In Commercial Distribution

  • 00888867295704 ()
AR-9564-2439-INF

  • Total reverse shoulder prosthesis
36 +4 LAT/24 Glenosphere
ARTHREX, INC.
AR-9564-2436-LAT
In Commercial Distribution

  • 00888867295681 ()
AR-9564-2436-LAT

  • Total reverse shoulder prosthesis
36 +2.5 INF/24 Glenosphere
ARTHREX, INC.
AR-9564-2436-INF
In Commercial Distribution

  • 00888867295674 ()
AR-9564-2436-INF

  • Total reverse shoulder prosthesis
33 +4 LAT/24 Glenosphere
ARTHREX, INC.
AR-9564-2433-LAT
In Commercial Distribution

  • 00888867295650 ()
AR-9564-2433-LAT

  • Total reverse shoulder prosthesis
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
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