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 Class Implantable

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PCM Breamer, Ø2.35 TPSE Sterile (US)
Nuvasive, Inc.
7679934P
In Commercial Distribution

  • 00887517403483 ()


  • Internal spinal fixation procedure kit, single-use
PCM Breamer, Ø2.35 JC Sterile (US)
Nuvasive, Inc.
7679930P
In Commercial Distribution

  • 00887517403476 ()


  • Internal spinal fixation procedure kit, single-use
PCM Breamer, Ø2.35 HXS Sterile (US)
Nuvasive, Inc.
7679927P
In Commercial Distribution

  • 00887517403469 ()


  • Internal spinal fixation procedure kit, single-use
PCM Breamer, Ø2.35 MRL Sterile (US)
Nuvasive, Inc.
7679926P
In Commercial Distribution

  • 00887517403452 ()


  • Internal spinal fixation procedure kit, single-use
PCM Breamer, Ø2.35 ANS Sterile (US)
Nuvasive, Inc.
7679925P
In Commercial Distribution

  • 00887517403445 ()


  • Internal spinal fixation procedure kit, single-use
PCM Breamer, Ø3.15mm MRC Sterile (US)
Nuvasive, Inc.
7679922P
In Commercial Distribution

  • 00887517403438 ()


  • Internal spinal fixation procedure kit, single-use
MaXcess 4 Light Cable
Nuvasive, Inc.
3241002
In Commercial Distribution

  • 00887517497222 ()


  • Surgical instrument fibreoptic light
CoRoent LO Titanium, 9x10x25 5°
Nuvasive, Inc.
6080925P
In Commercial Distribution

  • 00887517476357 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 8x10x40 5°
Nuvasive, Inc.
6080840P
In Commercial Distribution

  • 00887517476340 ()


  • Metallic spinal interbody fusion cage
CoRoent LO Titanium, 8x10x35 5°
Nuvasive, Inc.
6080835P
In Commercial Distribution

  • 00887517476333 ()


  • Metallic spinal interbody fusion cage
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