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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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VEO,TRIAL,0 DEG,17X7.5
Choice Spine, LP
V070-01775
In Commercial Distribution

  • 00840996132435 ()


  • Polymeric spinal interbody fusion cage
LATERAL,TRIAL,0 DEG,17X15
Choice Spine, LP
V070-01715
In Commercial Distribution

  • 00840996132428 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,0 DEG,17X13
Choice Spine, LP
V070-01713
In Commercial Distribution

  • 00840996132411 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,0 DEG,17X11
Choice Spine, LP
V070-01711
In Commercial Distribution

  • 00840996132404 ()


  • Polymeric spinal interbody fusion cage
VEO,TRIAL,0 DEG,17X9
Choice Spine, LP
V070-01709
In Commercial Distribution

  • 00840996132398 ()


  • Polymeric spinal interbody fusion cage
22x60x16mm - 0° PEEK 2C Cage
PRECISION SPINE, INC.
23-PC2260-16-2C
In Commercial Distribution

  • 00840019930710 ()
23-PC2260-16-2C

  • Polymeric spinal interbody fusion cage
22x60x12mm - 0° PEEK 2C Cage
PRECISION SPINE, INC.
23-PC2260-12-2C
In Commercial Distribution

  • 00840019930697 ()
23-PC2260-12-2C

  • Polymeric spinal interbody fusion cage
18x60x16mm - 0° PEEK 2C Cage
PRECISION SPINE, INC.
23-PC1860-16-2C
In Commercial Distribution

  • 00840019930512 ()
23-PC1860-16-2C

  • Polymeric spinal interbody fusion cage
18x60x12mm - 0° PEEK 2C Cage
PRECISION SPINE, INC.
23-PC1860-12-2C
In Commercial Distribution

  • 00840019930499 ()
23-PC1860-12-2C

  • Polymeric spinal interbody fusion cage
18x60x10mm - 0° PEEK 2C Cage
PRECISION SPINE, INC.
23-PC1860-10-2C
In Commercial Distribution

  • 00840019930482 ()
23-PC1860-10-2C

  • Polymeric spinal interbody fusion cage
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