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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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TLIF(B) Trial L28 x W10 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206147 ()
TI.2034

  • Spinal implant trial
TLIF(B) Trial L28 x W10 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206130 ()
TI.2033

  • Spinal implant trial
TLIF(B) Trial L28 x W10 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206123 ()
TI.2032

  • Spinal implant trial
TLIF(B) Trial L28 x W10 x H7
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206116 ()
TI.2031

  • Spinal implant trial
TLIF(B) Trial L36 x W9 x H16
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206109 ()
TI.2030

  • Spinal implant trial
TLIF(B) Trial L36 x W9 x H15
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206093 ()
TI.2029

  • Spinal implant trial
TLIF(B) Trial L36 x W9 x H14
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206086 ()
TI.2028

  • Spinal implant trial
TLIF(B) Trial L36 x W9 x H13
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206079 ()
TI.2027

  • Spinal implant trial
TLIF(B) Trial L36 x W9 x H12
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206062 ()
TI.2026

  • Spinal implant trial
TLIF(B) Trial L36 x W9 x H11
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206055 ()
TI.2025

  • Spinal implant trial
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