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 Type Device Class Implantable

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HI-LINE CRANIOTOME CUTTER II
Aesculap AG
GD805R
In Commercial Distribution

  • 04038653075621 ()
GD805R

  • Orthopaedic bur, reusable
HI-LINE DIAMOND BURR I D6.0MM
Aesculap AG
GD801R
In Commercial Distribution

  • 04038653075584 ()
GD801R

  • Orthopaedic bur, reusable
HI-LINE DIAMOND BURR III D3.1MM
Aesculap AG
GD797R
In Commercial Distribution

  • 04038653075546 ()
GD797R

  • Orthopaedic bur, reusable
HI-LINE DIAMOND BURR II D3.1MM
Aesculap AG
GD796R
In Commercial Distribution

  • 04038653075539 ()
GD796R

  • Orthopaedic bur, reusable
HI-LINE DIAMOND BURR II D1.4MM
Aesculap AG
GD790R
In Commercial Distribution

  • 04038653075478 ()
GD790R

  • Orthopaedic bur, reusable
HI-LINE DIAMOND BURR II D1.0MM
Aesculap AG
GD787R
In Commercial Distribution

  • 04038653075447 ()
GD787R

  • Orthopaedic bur, reusable
HI-LINE XS DISP.ROSEN BURR II D6.0MM
Aesculap AG
GE509SU
In Commercial Distribution

  • 04038653399154 ()
GE509SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR II D5.0MM
Aesculap AG
GE508SU
In Commercial Distribution

  • 04038653399147 ()
GE508SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR II D4.0MM
Aesculap AG
GE507SU
In Commercial Distribution

  • 04038653399130 ()
GE507SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR II D1.4MM
Aesculap AG
GE502SU
In Commercial Distribution

  • 04038653399079 ()
GE502SU

  • Orthopaedic bur, single-use
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