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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 L38 x W9 x H14
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206581 ()
TI.2098

  • Spinal implant trial
TLIF(B) Trial L38 x W9 x H13
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206574 ()
TI.2097

  • Spinal implant trial
TLIF(B) Trial L38 x W9 x H12
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206567 ()
TI.2096

  • Spinal implant trial
TLIF(B) Trial L38 x W9 x H11
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206550 ()
TI.2095

  • Spinal implant trial
TLIF(B) Trial L38 x W9 x H10
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206543 ()
TI.2094

  • Spinal implant trial
TLIF(B) Trial L38 x W9 x H9
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206536 ()
TI.2093

  • Spinal implant trial
TLIF(B) Trial L38 x W9 x H8
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206529 ()
TI.2092

  • Spinal implant trial
TLIF(B) Trial L38 x W9 x H7
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206512 ()
TI.2091

  • Spinal implant trial
TLIF(B) Trial L28 x W11 x H16
DIOMEDICAL CO.,LTD.
A
In Commercial Distribution

  • 08809557206505 ()
TI.2070

  • Spinal implant trial
REESE OSTEOTOMY GUIDE SYSTEM: PART B: MAP LOG
ELMED INCORPORATED
ST230819B
In Commercial Distribution

  • 00842180194984 ()
ST230819B

  • Orthopaedic surgical procedure kit, non-medicated, reusable
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