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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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CURETTE X0512054 3.6MM STRAIGHT
MEDTRONIC SOFAMOR DANEK, INC.
X0512054
Not in Commercial Distribution

  • 00643169183117 ()


  • Bone curette, reusable
CURETTE X0512053 1.8MM REVERSE
MEDTRONIC SOFAMOR DANEK, INC.
X0512053
In Commercial Distribution

  • 00643169183100 ()


  • Bone curette, reusable
CURETTE X0512052 1.8MM ANGLED
MEDTRONIC SOFAMOR DANEK, INC.
X0512052
In Commercial Distribution

  • 00643169183094 ()


  • Bone curette, reusable
CURETTE X0512051 1.8MM STRAIGHT
MEDTRONIC SOFAMOR DANEK, INC.
X0512051
In Commercial Distribution

  • 00643169183087 ()


  • Bone curette, reusable
PITUITARY X0512063 4MM
MEDTRONIC SOFAMOR DANEK, INC.
X0512063
In Commercial Distribution

  • 00643169183070 ()


  • Orthopaedic joint/limb rongeur
KERRISON X0512075 5MM, 90
MEDTRONIC SOFAMOR DANEK, INC.
X0512075
In Commercial Distribution

  • 00643169183063 ()


  • Bone curette, reusable
KERRISON X0512074 5MM, 40
MEDTRONIC SOFAMOR DANEK, INC.
X0512074
In Commercial Distribution

  • 00643169183056 ()


  • Bone curette, reusable
KERRISON X0512073 4MM, 90
MEDTRONIC SOFAMOR DANEK, INC.
X0512073
In Commercial Distribution

  • 00643169183049 ()


  • Bone curette, reusable
KERRISON X0512072 4MM, 40
MEDTRONIC SOFAMOR DANEK, INC.
X0512072
In Commercial Distribution

  • 00643169183032 ()


  • Bone curette, reusable
KERRISON X0512071 3MM, 90
MEDTRONIC SOFAMOR DANEK, INC.
X0512071
In Commercial Distribution

  • 00643169183025 ()


  • Bone curette, reusable
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