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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 ALIF Interbody, 10x38x28mm 20°
Nuvasive, Inc.
1908820P2
In Commercial Distribution

  • 00195377067128 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x26x22mm 20°
Nuvasive, Inc.
1906220P2
In Commercial Distribution

  • 00195377067098 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 10x42x32mm 20°
Nuvasive, Inc.
1902020P2
In Commercial Distribution

  • 00195377067012 ()


  • Polymeric spinal interbody fusion cage
VALEO Corpectomy 16x12, 20, 6deg
CTL Medical Corporation
11.009.1620
In Commercial Distribution



  • Polymeric spinal interbody fusion cage
VALEO Corpectomy 17x14, 20, 6deg
CTL Medical Corporation
11.009.2620
In Commercial Distribution

  • 00841732144897 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x38x28mm 20°
Nuvasive, Inc.
1988820P2
In Commercial Distribution

  • 00195377067654 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x26x22mm 20°
Nuvasive, Inc.
1986220P2
In Commercial Distribution

  • 00195377067623 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x34x24mm 20°
Nuvasive, Inc.
1984420P2
In Commercial Distribution

  • 00195377067579 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 8x42x32mm 20°
Nuvasive, Inc.
1982020P2
In Commercial Distribution

  • 00195377067524 ()


  • Polymeric spinal interbody fusion cage
COHERE ALIF Interbody, 7x26x22mm 20°
Nuvasive, Inc.
1976220P2
In Commercial Distribution

  • 00195377067494 ()


  • Polymeric spinal interbody fusion cage
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