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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 - 00887517702418

BASE HL Trial, 8x42x30mm 20°
Nuvasive, Inc.
6956820
In Commercial Distribution

  • 00887517702418 ()


  • Spinal implant trial

BASE - 00887517702364

BASE HL Trial, 6x42x30mm 20°
Nuvasive, Inc.
6956620
In Commercial Distribution

  • 00887517702364 ()


  • Spinal implant trial

BASE - 00887517702319

BASE HL Trial, 4x42x30mm 20°
Nuvasive, Inc.
6956420
In Commercial Distribution

  • 00887517702319 ()


  • Spinal implant trial

BASE - 00887517701701

BASE HL Trial, 10x38x28mm 20°
Nuvasive, Inc.
6955020
In Commercial Distribution

  • 00887517701701 ()


  • Spinal implant trial

BASE - 00887517701657

BASE HL Trial, 8x34x24mm 20°
Nuvasive, Inc.
6954820
In Commercial Distribution

  • 00887517701657 ()


  • Spinal implant trial

BASE - 00887517701459

BASE HL Trial, 12x34x24mm 20°
Nuvasive, Inc.
6954220
In Commercial Distribution

  • 00887517701459 ()


  • Spinal implant trial

BASE - 00887517701404

BASE HL Trial, 10x34x24mm 20°
Nuvasive, Inc.
6954020
In Commercial Distribution

  • 00887517701404 ()


  • Spinal implant trial

BASE - 00887517701602

BASE HL Trial, 6x34x24mm 20°
Nuvasive, Inc.
6954620
In Commercial Distribution

  • 00887517701602 ()


  • Spinal implant trial

BASE - 00887517701558

BASE HL Trial, 4x34x24mm 20°
Nuvasive, Inc.
6954420
In Commercial Distribution

  • 00887517701558 ()


  • Spinal implant trial

BASE - 00887517701503

BASE HL Trial, 14x34x24mm 20°
Nuvasive, Inc.
6954320
In Commercial Distribution

  • 00887517701503 ()


  • Spinal implant trial
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