SEARCH RESULTS FOR: ("源头企业签名[Contact Telegram: duo785].hfs")(34366 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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Modular Tibia Augment Size 2 x 4mm
Omni Life Science, Inc.
KC-54020
In Commercial Distribution

  • 00841690111788 ()
KC-54020

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

  • 00841690111771 ()
KC-54010

  • Knee arthroplasty wedge
Modular Tibia Augment Bolt Size 12mm
Omni Life Science, Inc.
KC-53112
In Commercial Distribution

  • 00841690111757 ()
KC-53112

  • Knee arthroplasty wedge
Modular Tibia Augment Bolt Size 8mm
Omni Life Science, Inc.
KC-53108
In Commercial Distribution

  • 00841690111740 ()
KC-53108

  • Knee arthroplasty wedge
Modular Tibia Augment Bolt Size 4mm
Omni Life Science, Inc.
KC-53104
In Commercial Distribution

  • 00841690111733 ()
KC-53104

  • Knee arthroplasty wedge
Femoral Segment
WALDEMAR LINK GmbH & Co. KG
15-2962/19
In Commercial Distribution

  • 04026575214204 ()
15-2962/19

  • Knee arthroplasty wedge
Femoral Segment
WALDEMAR LINK GmbH & Co. KG
15-2962/18
In Commercial Distribution

  • 04026575214198 ()
15-2962/18

  • Knee arthroplasty wedge
Femoral Segment
WALDEMAR LINK GmbH & Co. KG
15-2962/17
In Commercial Distribution

  • 04026575214181 ()
15-2962/17

  • Knee arthroplasty wedge
Femoral Segment
WALDEMAR LINK GmbH & Co. KG
15-2962/16
In Commercial Distribution

  • 04026575214174 ()
15-2962/16

  • Knee arthroplasty wedge
Femoral Segment
WALDEMAR LINK GmbH & Co. KG
15-2962/15
In Commercial Distribution

  • 04026575214167 ()
15-2962/15

  • Knee arthroplasty wedge
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