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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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Size 6 Tibial Augment Wedge 10 Degrees RT Lat/LT Med
Ortho Development Corporation
567-1106
In Commercial Distribution

  • 00822409003457 ()

  • Angle: 10 degree


  • Knee arthroplasty wedge
Size 5 Tibial Augment Wedge 10 Degrees RT Lat/LT Med
Ortho Development Corporation
567-1105
In Commercial Distribution

  • 00822409003440 ()

  • Angle: 10 degree


  • Knee arthroplasty wedge
Size 4 Tibial Augment Wedge 10 Degrees RT Lat/LT Med
Ortho Development Corporation
567-1104
In Commercial Distribution

  • 00822409003433 ()

  • Angle: 10 degree


  • Knee arthroplasty wedge
Size 3 Tibial Augment Wedge 10 Degrees RT Lat/LT Med
Ortho Development Corporation
567-1103
In Commercial Distribution

  • 00822409003426 ()

  • Angle: 10 degree


  • Knee arthroplasty wedge
Size 2 Tibial Augment Wedge 10 Degrees RT Lat/LT Med
Ortho Development Corporation
567-1102
In Commercial Distribution

  • 00822409003419 ()

  • Angle: 10 degree


  • Knee arthroplasty wedge
Size 1 Tibial Augment Wedge 10 Degrees RT Lat/LT Med
Ortho Development Corporation
567-1101
In Commercial Distribution

  • 00822409003402 ()

  • Angle: 10 degree


  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5990-35-24
In Commercial Distribution

  • 00889024563896 ()

  • Size E, 20 mm Augment
00-5990-035-24

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5990-35-02
In Commercial Distribution

  • 00889024563889 ()

  • Size E, 10 mm Augment
00-5990-035-02

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5990-34-21
In Commercial Distribution

  • 00889024563872 ()

  • Size D, 10 mm Augment
00-5990-034-21

  • Knee arthroplasty wedge
No Description
Zimmer, Inc.
5990-34-10
In Commercial Distribution

  • 00889024563865 ()

  • Size D, 5 mm Augment
00-5990-034-10

  • Knee arthroplasty wedge
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