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 Class Implantable

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ALIF Interfixated Guide, L
Nuvasive, Inc.
1770801
In Commercial Distribution

  • 00887517640178 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, J
Nuvasive, Inc.
1770799
In Commercial Distribution

  • 00887517640161 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, I
Nuvasive, Inc.
1770798
In Commercial Distribution

  • 00887517640154 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, H
Nuvasive, Inc.
1770797
In Commercial Distribution

  • 00887517640147 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, G
Nuvasive, Inc.
1770796
In Commercial Distribution

  • 00887517640130 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, F
Nuvasive, Inc.
1770795
In Commercial Distribution

  • 00887517640123 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, E
Nuvasive, Inc.
1770794
In Commercial Distribution

  • 00887517640116 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, D
Nuvasive, Inc.
1770793
In Commercial Distribution

  • 00887517640109 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, C
Nuvasive, Inc.
1770792
In Commercial Distribution

  • 00887517640093 ()


  • Surgical instrument/implant depth limiter
ALIF Interfixated Guide, B
Nuvasive, Inc.
1770791
In Commercial Distribution

  • 00887517640086 ()


  • Surgical instrument/implant depth limiter
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