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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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Interlock HL, 16x17x14mm 20°
Nuvasive, Inc.
1662344
In Commercial Distribution

  • 00887517711830 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 15x17x14mm 20°
Nuvasive, Inc.
1662340
In Commercial Distribution

  • 00887517711793 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 14x17x14mm 20°
Nuvasive, Inc.
1662333
In Commercial Distribution

  • 00887517711748 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 13x17x14mm 20°
Nuvasive, Inc.
1662328
In Commercial Distribution

  • 00887517711694 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 12x17x14mm 20°
Nuvasive, Inc.
1662323
In Commercial Distribution

  • 00887517711649 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 11x17x14mm 20°
Nuvasive, Inc.
1662318
In Commercial Distribution

  • 00887517711595 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 10x17x14mm 20°
Nuvasive, Inc.
1662314
In Commercial Distribution

  • 00887517711557 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 9x17x14mm 20°
Nuvasive, Inc.
1662310
In Commercial Distribution

  • 00887517711519 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 8x17x14mm 20°
Nuvasive, Inc.
1662307
In Commercial Distribution

  • 00887517711281 ()


  • Polymeric spinal interbody fusion cage
CURRETTE X8750314 ANGLED 2-0
MEDTRONIC SOFAMOR DANEK, INC.
X8750314
Not in Commercial Distribution

  • 00885074234250 ()


  • Bone curette, reusable
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