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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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Cohere TLIF-A, 11x9x30mm 15°
Nuvasive, Inc.
4119305P2
In Commercial Distribution

  • 00195377029515 ()


  • Polymeric spinal interbody fusion cage
Cohere TLIF-A, 11x14x30mm 8°
Nuvasive, Inc.
4114308P2
In Commercial Distribution

  • 00195377029508 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLR, 10x26x22mm 10°
Nuvasive, Inc.
6961062
In Commercial Distribution

  • 00195377029492 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLR, 8x26x22mm 10°
Nuvasive, Inc.
6960862
In Commercial Distribution

  • 00195377029485 ()


  • Polymeric spinal interbody fusion cage
CoRoent XLR, 6x26x22mm 10°
Nuvasive, Inc.
6960662
In Commercial Distribution

  • 00195377029478 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 18x10x30mm 12°
Nuvasive, Inc.
6180302P2
In Commercial Distribution

  • 00195377036018 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x14x30mm 4°
Nuvasive, Inc.
6124304P2
In Commercial Distribution

  • 00195377034991 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x10x30mm 8°
Nuvasive, Inc.
6120308P2
In Commercial Distribution

  • 00195377034984 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 12x10x25mm 8°
Nuvasive, Inc.
6120258P2
In Commercial Distribution

  • 00195377034977 ()


  • Polymeric spinal interbody fusion cage
COHERE TLIF-O, 11x10x30mm 8°
Nuvasive, Inc.
6110308P2
In Commercial Distribution

  • 00195377034960 ()


  • Polymeric spinal interbody fusion cage
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