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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 Class Implantable

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BONE RASP 8MM
Synthes GmbH
389.715
In Commercial Distribution

  • H9813897150 ()
  • 10705034776316 ()
389715

  • Bone file/rasp, manual, reusable
BONE RASP 8MM-STRAIGHT
Synthes GmbH
389.714
In Commercial Distribution

  • 07611819742765 ()
  • H9813897140 ()
  • 10705034776309 ()
389714

  • Bone file/rasp, manual, reusable
BONE RASP 8MM WIDTH-LEFT
Synthes GmbH
389.286
In Commercial Distribution

  • 07611819742147 ()
  • H9813892860 ()
  • 10705034775395 ()
389286

  • Bone file/rasp, manual, reusable
BONE RASP 8MM WIDTH-RIGHT
Synthes GmbH
389.285
In Commercial Distribution

  • 07611819742130 ()
  • H9813892850 ()
  • 10705034775388 ()
389285

  • Bone file/rasp, manual, reusable
ALIF RASP
Synthes GmbH
389.156
In Commercial Distribution

  • H9813891560 ()
  • 10705034774817 ()
389156

  • Bone file/rasp, manual, reusable
PLIF SPREADER/17MM
Synthes GmbH
389.117
In Commercial Distribution

  • H9813891170 ()
  • 10705034774619 ()
389117

  • Bone distraction forceps
PLIF SPREADER/15MM
Synthes GmbH
389.115
In Commercial Distribution

  • H9813891150 ()
  • 10705034774602 ()
389115

  • Bone distraction forceps
PLIF SPREADER/13MM
Synthes GmbH
389.113
In Commercial Distribution

  • H9813891130 ()
  • 10705034774596 ()
389113

  • Bone distraction forceps
PLIF SPREADER/11MM
Synthes GmbH
389.111
In Commercial Distribution

  • H9813891110 ()
  • 10705034774589 ()
389111

  • Bone distraction forceps
PLIF SPREADER/9MM
Synthes GmbH
389.109
In Commercial Distribution

  • H9813891090 ()
  • 10705034774572 ()
389109

  • Bone distraction forceps
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