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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 Class Implantable

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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
ALIF Interfixated Guide, A
Nuvasive, Inc.
1770790
In Commercial Distribution

  • 00887517640079 ()


  • Surgical instrument/implant depth limiter
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