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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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HYH,FLTR,RESP,WH,-,20
O&M HALYARD, INC.
62360
Not in Commercial Distribution

  • 30680651623608 ()
  • 20680651623601 ()
  • 90680651623600 ()
62360

  • Surgical/medical face mask, non-antimicrobial, single-use
Interlock II Ti-C, 15x17x14mm 20°
Nuvasive, Inc.
6771520CP2
In Commercial Distribution

  • 00887517812841 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 11x17x14mm 20°
Nuvasive, Inc.
6771120CP2
In Commercial Distribution

  • 00887517812605 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 16x19x16mm 20°
Nuvasive, Inc.
6779620CP2
In Commercial Distribution

  • 00887517813664 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 15x19x16mm 20°
Nuvasive, Inc.
6779520CP2
In Commercial Distribution

  • 00887517813602 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 14x19x16mm 20°
Nuvasive, Inc.
6779420CP2
In Commercial Distribution

  • 00887517813541 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 13x19x16mm 20°
Nuvasive, Inc.
6779320CP2
In Commercial Distribution

  • 00887517813480 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 12x19x16mm 20°
Nuvasive, Inc.
6779220CP2
In Commercial Distribution

  • 00887517813428 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 11x19x16mm 20°
Nuvasive, Inc.
6779120CP2
In Commercial Distribution

  • 00887517813374 ()


  • Polymeric spinal interbody fusion cage
Interlock II Ti-C, 10x19x16mm 20°
Nuvasive, Inc.
6779020CP2
In Commercial Distribution

  • 00887517813329 ()


  • Polymeric spinal interbody fusion cage
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