SEARCH RESULTS FOR: ("安卓應用加密[Contact Telegram: Heimaapp].ucb")(34143 results)

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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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No Description
Biomet Orthopedics, LLC
184280
In Commercial Distribution

  • 00880304433984 ()

  • 15 MM 55 MM
184280

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184285
In Commercial Distribution

  • 00880304433564 ()

  • 15 MM 67.5 MM
184285

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184181
In Commercial Distribution

  • 00880304433410 ()

  • 10 MM 57.5 MM
184181

  • Knee arthroplasty wedge
No Description
Biomet Orthopedics, LLC
184144
In Commercial Distribution

  • 00880304433403 ()

  • 5 MM 65 MM
184144

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT XLG NON-POROUS
Microport Orthopedics Inc.
18723012
In Commercial Distribution

  • 18723012 ()
  • M684187230121 ()
18723012

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT LG+ NON-POROUS
Microport Orthopedics Inc.
18723010
In Commercial Distribution

  • 18723010 ()
  • M684187230101 ()
18723010

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT LG NON-POROUS
Microport Orthopedics Inc.
18723008
In Commercial Distribution

  • 18723008 ()
  • M684187230081 ()
18723008

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT MD/MD+ NON-POROUS
Microport Orthopedics Inc.
18723004
In Commercial Distribution

  • 18723004 ()
  • M684187230041 ()
18723004

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT SM+ NON-POROUS
Microport Orthopedics Inc.
18723002
In Commercial Distribution

  • 18723002 ()
  • M684187230021 ()
18723002

  • Knee arthroplasty wedge
ADVANTIM® FEMORAL AUGMENT LG+ LT/MEDIAL RT/LATERAL
Microport Orthopedics Inc.
18722138
In Commercial Distribution

  • 18722138 ()
  • M684187221381 ()
18722138

  • Knee arthroplasty wedge
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