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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, 8x17x14mm 20°
Nuvasive, Inc.
1662307
In Commercial Distribution

  • 00887517711281 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 8x17x14mm 15°
Nuvasive, Inc.
1662306
In Commercial Distribution

  • 00887517711274 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 8x17x14mm 10°
Nuvasive, Inc.
1662305
In Commercial Distribution

  • 00887517711267 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 7x17x14mm 15°
Nuvasive, Inc.
1662304
In Commercial Distribution

  • 00887517711250 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 7x17x14mm 10°
Nuvasive, Inc.
1662303
In Commercial Distribution

  • 00887517711243 ()


  • Polymeric spinal interbody fusion cage
Interlock HL, 6x17x14mm 10°
Nuvasive, Inc.
1662302
In Commercial Distribution

  • 00887517711236 ()


  • Polymeric spinal interbody fusion cage
COALESCE Straight, 10x9x23mm 8°
Nuvasive, Inc.
4109238P2
In Commercial Distribution

  • 00887517056481 ()


  • Polymeric spinal interbody fusion cage
COALESCE Straight, 9x10x28mm 8°
Nuvasive, Inc.
4090288P2
In Commercial Distribution

  • 00887517056399 ()


  • Polymeric spinal interbody fusion cage
COALESCE Straight, 8x9x23mm 8°
Nuvasive, Inc.
4089238P2
In Commercial Distribution

  • 00887517056382 ()


  • Polymeric spinal interbody fusion cage
COALESCE Straight, 8x9x23mm 0°
Nuvasive, Inc.
1007849
In Commercial Distribution

  • 00887517056375 ()


  • Polymeric spinal interbody fusion cage
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