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 XS DISP.DIAMOND BURR XL-I D4.0MM
Aesculap AG
GE717SU
In Commercial Distribution

  • 04038653469833 ()
GE717SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR XL-I D3.1MM
Aesculap AG
GE716SU
Not in Commercial Distribution

  • 04038653469826 ()
GE716SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR XL-I D2.3MM
Aesculap AG
GE714SU
In Commercial Distribution

  • 04038653469819 ()
GE714SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-I D6.0MM
Aesculap AG
GE709SU
Not in Commercial Distribution

  • 04038653469758 ()
GE709SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-I D5.0MM
Aesculap AG
GE708SU
In Commercial Distribution

  • 04038653469741 ()
GE708SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-I D4.0MM
Aesculap AG
GE707SU
Not in Commercial Distribution

  • 04038653469734 ()
GE707SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-I D3.1MM
Aesculap AG
GE706SU
Not in Commercial Distribution

  • 04038653469727 ()
GE706SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-I D2.3MM
Aesculap AG
GE704SU
Not in Commercial Distribution

  • 04038653469710 ()
GE704SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TWIST DRILL/GB740R D1.5
Aesculap AG
GE395SU
In Commercial Distribution

  • 04038653463404 ()
GE395SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TWIST DRILL/GB740R D1.1
Aesculap AG
GE391SU
In Commercial Distribution

  • 04038653463381 ()
GE391SU

  • Orthopaedic bur, single-use
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