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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 Class Implantable

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Cross-Link, 50mm
BK MEDITECH CO.,LTD.
61510-50
In Commercial Distribution

  • 08809155852586 ()


  • Bone-screw internal spinal fixation system, non-sterile
Cross-Link, 45mm
BK MEDITECH CO.,LTD.
61510-45
In Commercial Distribution

  • 08809155852579 ()


  • Bone-screw internal spinal fixation system, non-sterile
Cross-Link, 40mm
BK MEDITECH CO.,LTD.
61510-40
In Commercial Distribution

  • 08809155852562 ()


  • Bone-screw internal spinal fixation system, non-sterile
Cross-Link, 35mm
BK MEDITECH CO.,LTD.
61510-35
In Commercial Distribution

  • 08809155852555 ()


  • Bone-screw internal spinal fixation system, non-sterile
Dyna-EXTOR(ST) Ⅱ, 3.0cm
BK MEDITECH CO.,LTD.
25400
In Commercial Distribution

  • 08809155852531 ()


  • External orthopaedic fixation system, single-use
Dyna-EXTOR(ST) Ⅱ, 3.6cm
BK MEDITECH CO.,LTD.
25300
In Commercial Distribution

  • 08809155852524 ()


  • External orthopaedic fixation system, single-use
Dyna-EXTOR(ST) Ⅱ, 7.0cm
BK MEDITECH CO.,LTD.
25310-07
In Commercial Distribution

  • 08809155852517 ()


  • External orthopaedic fixation system, single-use
Dyna-EXTOR(ST) Ⅱ, 6.0cm
BK MEDITECH CO.,LTD.
25310-06
In Commercial Distribution

  • 08809155852500 ()


  • External orthopaedic fixation system, single-use
Pre-bent Rod, Ø6.0 x 100mm
BK MEDITECH CO.,LTD.
61121-100
In Commercial Distribution

  • 08809155852470 ()


  • Bone-screw internal spinal fixation system, non-sterile
Pre-bent Rod, Ø6.0 x 90mm
BK MEDITECH CO.,LTD.
61121-090
In Commercial Distribution

  • 08809155852463 ()


  • Bone-screw internal spinal fixation system, non-sterile
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