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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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High Performance Revision Tibia Augment, Size 4 x 4mm
Omni Life Science, Inc.
KC-54040-HP
In Commercial Distribution

  • 00841690131083 ()
KC-54040-HP

  • Knee arthroplasty wedge
High Performance Revision Tibia Augment, Size 3 x 4mm
Omni Life Science, Inc.
KC-54030-HP
In Commercial Distribution

  • 00841690131069 ()
KC-54030-HP

  • Knee arthroplasty wedge
High Performance Revision Tibia Augment, Size 2 x 4mm
Omni Life Science, Inc.
KC-54020-HP
In Commercial Distribution

  • 00841690131045 ()
KC-54020-HP

  • Knee arthroplasty wedge
High Performance Revision Tibia Augment, Size 1 x 4mm
Omni Life Science, Inc.
KC-54010-HP
In Commercial Distribution

  • 00841690131021 ()
KC-54010-HP

  • Knee arthroplasty wedge
Revision Tibia Augment Peg Bolt Size 12mm
Omni Life Science, Inc.
KC-53312
In Commercial Distribution

  • 00841690129011 ()
KC-53312

  • Knee arthroplasty wedge
Revision Tibia Augment Peg Bolt Size 8mm
Omni Life Science, Inc.
KC-53308
In Commercial Distribution

  • 00841690129004 ()
KC-53308

  • Knee arthroplasty wedge
Revision Tibia Augment Peg Bolt Size 4mm
Omni Life Science, Inc.
KC-53304
In Commercial Distribution

  • 00841690128991 ()
KC-53304

  • Knee arthroplasty wedge
Femoral Augment, Notched Posterior, Size 1, 10mm
Omni Life Science, Inc.
KP-31101
In Commercial Distribution

  • 00841690128960 ()
KP-31101

  • Knee arthroplasty wedge
Femoral Augment, Notched Posterior, Size 5+, 10mm
Omni Life Science, Inc.
KP-45101
In Commercial Distribution

  • 00841690128953 ()
KP-45101

  • Knee arthroplasty wedge
Femoral Augment, Notched Posterior, Size 4+, 10mm
Omni Life Science, Inc.
KP-44101
In Commercial Distribution

  • 00841690128946 ()
KP-44101

  • Knee arthroplasty wedge
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