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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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BASE - 00887517705037

BASE HL Trial, 12x42x36mm 20°
Nuvasive, Inc.
6959261
In Commercial Distribution

  • 00887517705037 ()


  • Spinal implant trial

BASE - 00887517705020

BASE HL Trial, 10x42x36mm 20°
Nuvasive, Inc.
6959260
In Commercial Distribution

  • 00887517705020 ()


  • Spinal implant trial

BASE - 00887517705006

BASE HL Trial, 6x42x36mm 20°
Nuvasive, Inc.
6959258
In Commercial Distribution

  • 00887517705006 ()


  • Spinal implant trial

BASE - 00887517704993

BASE HL Trial, 4x42x36mm 20°
Nuvasive, Inc.
6959257
In Commercial Distribution

  • 00887517704993 ()


  • Spinal implant trial

BASE - 00887517704467

BASE HL Trial, 8x42x32mm 20°
Nuvasive, Inc.
6959204
In Commercial Distribution

  • 00887517704467 ()


  • Spinal implant trial

BASE - 00887517704450

BASE HL Trial, 6x42x32mm 20°
Nuvasive, Inc.
6959203
In Commercial Distribution

  • 00887517704450 ()


  • Spinal implant trial

BASE - 00887517704009

BASE HL Trial, 14x38x36mm 20°
Nuvasive, Inc.
6959152
In Commercial Distribution

  • 00887517704009 ()


  • Spinal implant trial

BASE - 00887517703996

BASE HL Trial, 12x38x36mm 20°
Nuvasive, Inc.
6959151
In Commercial Distribution

  • 00887517703996 ()


  • Spinal implant trial

BASE - 00887517703972

BASE HL Trial, 8x38x36mm 20°
Nuvasive, Inc.
6959149
In Commercial Distribution

  • 00887517703972 ()


  • Spinal implant trial

BASE - 00887517703965

BASE HL Trial, 6x38x36mm 20°
Nuvasive, Inc.
6959148
In Commercial Distribution

  • 00887517703965 ()


  • Spinal implant trial
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