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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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MectaLIF Posterior PEEK 9x25x13 L12°
Medacta International SA
03.21.244
In Commercial Distribution

  • 07630345728388 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x25x12 L12°
Medacta International SA
03.21.243
In Commercial Distribution

  • 07630345728371 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x22x15 L12°
Medacta International SA
03.21.242
In Commercial Distribution

  • 07630345728364 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x22x14 L12°
Medacta International SA
03.21.241
In Commercial Distribution

  • 07630345728357 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x22x13 L12°
Medacta International SA
03.21.240
In Commercial Distribution

  • 07630345728340 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x22x12 L12°
Medacta International SA
03.21.239
In Commercial Distribution

  • 07630345728333 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x22x11 L12°
Medacta International SA
03.21.238
In Commercial Distribution

  • 07630345728326 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x19x15 L12°
Medacta International SA
03.21.237
In Commercial Distribution

  • 07630345728319 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x19x14 L12°
Medacta International SA
03.21.236
In Commercial Distribution

  • 07630345728302 ()


  • Metallic spinal interbody fusion cage
MectaLIF Posterior PEEK 9x19x13 L12°
Medacta International SA
03.21.235
In Commercial Distribution

  • 07630345728296 ()


  • Metallic spinal interbody fusion cage
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