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.BARREL BURR XL-I D6.0MM
Aesculap AG
GE712SU
In Commercial Distribution

  • 04038653469895 ()
GE712SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.BARREL BURR XL-I D4.0MM
Aesculap AG
GE711SU
Not in Commercial Distribution

  • 04038653469888 ()
GE711SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR XL-I D6.0MM
Aesculap AG
GE719SU
Not in Commercial Distribution

  • 04038653469857 ()
GE719SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR XL-I D5.0MM
Aesculap AG
GE718SU
In Commercial Distribution

  • 04038653469840 ()
GE718SU

  • Orthopaedic bur, single-use
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
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