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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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Trial Augment 70/72 20
Medacta International SA
01.38.10.7020
In Commercial Distribution

  • 07630040761017 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Trial Augment 66/68 20
Medacta International SA
01.38.10.6620
In Commercial Distribution

  • 07630040760980 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
Trial Augment 62/64 20
Medacta International SA
01.38.10.6220
In Commercial Distribution

  • 07630040760959 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
KNEE IMMOBILIZER, XL 20 IN
DJO, LLC
155-79-96019
In Commercial Distribution

  • 00190446660538 ()


  • Knee immobilizer
THUNDERBOLT,KWIRE,SS,TROCAR-TROCAR,20"
Choice Spine, LP
M070-KS320
In Commercial Distribution

  • 00840996135795 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,SS,BLUNT-TROCAR,20"
Choice Spine, LP
M070-KS220
In Commercial Distribution

  • 00840996135757 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,SS,BLUNT-BLUNT,20"
Choice Spine, LP
M070-KS120
In Commercial Distribution

  • 00840996135719 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,NITL,TROCAR-TROCAR,20"
Choice Spine, LP
M070-KN320
In Commercial Distribution

  • 00840996135672 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,NITOL,BLUNT-TROCAR,20"
Choice Spine, LP
M070-KN220
In Commercial Distribution

  • 00840996135634 ()


  • Bone-screw internal spinal fixation system, non-sterile
THUNDERBOLT,KWIRE,NITOL,BLUNT-BLUNT,20"
Choice Spine, LP
M070-KN120
In Commercial Distribution

  • 00840996135597 ()


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