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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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Reusable instrument for Total Knee Arthroplasty
PIXEE MEDICAL
Knee+
In Commercial Distribution

  • 03760297030070 ()
KNI009

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reusable instrument for Total Knee Arthroplasty
PIXEE MEDICAL
Knee+
In Commercial Distribution

  • 03760297030063 ()
KNI008

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reusable instrument for Total Knee Arthroplasy
PIXEE MEDICAL
Knee+
In Commercial Distribution

  • 03760297030056 ()
KNI007

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reusable instrument for Total Knee Arthroplasty
PIXEE MEDICAL
Knee+
In Commercial Distribution

  • 03760297030049 ()
KNI006

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reusable instrument for Total Knee Arthroplasty
PIXEE MEDICAL
Knee+
In Commercial Distribution

  • 03760297030032 ()
KNI005

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reusable instrument for Total Knee Arthroplasty
PIXEE MEDICAL
Knee+
In Commercial Distribution

  • 03760297030001 ()
KNI001

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Kit, 2.5mm Guide Pin (5 Pk)
ARTHROSURFACE INCORPORATED
8007-1205
In Commercial Distribution

  • M528800712050 ()
8007-1205

  • Orthopaedic bone wire
Guide, ANKLE, Nano Fracture
ARTHROSURFACE INCORPORATED
5500-4010
In Commercial Distribution

  • M528550040100 ()
5500-4010

  • Subchondral bone needling device handle
Guide, Hip, 15o Nanofracture
ARTHROSURFACE INCORPORATED
5500-3310
In Commercial Distribution

  • M528550033100 ()
5500-3310

  • Subchondral bone needling device handle
NanoFx, Guide, 15 Degree
ARTHROSURFACE INCORPORATED
5500-1020
In Commercial Distribution

  • M528550010200 ()
5500-1020

  • Subchondral bone needling device handle
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