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-3 D6.0MM
Aesculap AG
GE294SU
In Commercial Distribution

  • 04038653470105 ()
GE294SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR XL-3 D3.1MM
Aesculap AG
GE293SU
In Commercial Distribution

  • 04038653470068 ()
GE293SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-3 D6.0MM
Aesculap AG
GE291SU
In Commercial Distribution

  • 04038653470020 ()
GE291SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-3 D3.1MM
Aesculap AG
GE290SU
Not in Commercial Distribution

  • 04038653469987 ()
GE290SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ACTIV C DRILL XL-I D1.5
Aesculap AG
GE700SU
In Commercial Distribution

  • 04038653469932 ()
GE700SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.NEURO CUTTER XL-I D3.1MM
Aesculap AG
GE702SU
In Commercial Distribution

  • 04038653469918 ()
GE702SU

  • Orthopaedic bur, single-use
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
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