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 BARREL BURR II D5.0MM
Aesculap AG
GD845R
In Commercial Distribution

  • 04038653279913 ()
GD845R

  • Orthopaedic bur, reusable
HI-LINE CONE BURR II D7.0MM
Aesculap AG
GD843R
Not in Commercial Distribution

  • 04038653279890 ()
GD843R

  • Orthopaedic bur, reusable
HI-LINE CONE BURR II D5.0MM
Aesculap AG
GD841R
In Commercial Distribution

  • 04038653279876 ()
GD841R

  • Orthopaedic bur, reusable
HI-LINE XS DISP.DIAMOND BURR II D3.1MM
Aesculap AG
GE516SU
In Commercial Distribution

  • 04038653399208 ()
GE516SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR II D2.3MM
Aesculap AG
GE514SU
In Commercial Distribution

  • 04038653399192 ()
GE514SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR II D1.8MM
Aesculap AG
GE513SU
In Commercial Distribution

  • 04038653399185 ()
GE513SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR II D1.4MM
Aesculap AG
GE512SU
In Commercial Distribution

  • 04038653399178 ()
GE512SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR II D1.0MM
Aesculap AG
GE511SU
In Commercial Distribution

  • 04038653399161 ()
GE511SU

  • Orthopaedic bur, single-use
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
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