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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ELAN 4 1-RING ROSEN BURR+ D2.7
Aesculap AG
GP123R
Not in Commercial Distribution

  • 04046964558962 ()
GP123R

  • Orthopaedic bur, reusable
ELAN 4 1-RING ROSEN BURR TC D2.0
Aesculap AG
GP119TC
Not in Commercial Distribution

  • 04046964558924 ()
GP119TC

  • Orthopaedic bur, reusable
ELAN 4 1-RING ROSEN BURR D1.8
Aesculap AG
GP117R
Not in Commercial Distribution

  • 04046964558900 ()
GP117R

  • Orthopaedic bur, reusable
ELAN 4 1-RING TWIN CUT BURR D4.0
Aesculap AG
GP184R
In Commercial Distribution

  • 04046964558887 ()
GP184R

  • Orthopaedic bur, reusable
HI-LINE XS DISP.DIAMOND BURR XL-3 D4.5MM
Aesculap AG
GE296SU
In Commercial Distribution

  • 04046963519216 ()
GE296SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR XL-2 D4.5MM
Aesculap AG
GE286SU
In Commercial Distribution

  • 04046963519209 ()
GE286SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR XL-3 D4.5MM
Aesculap AG
GE292SU
In Commercial Distribution

  • 04046963519193 ()
GE292SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I+ D2.3MM
Aesculap AG
GE464SU
Not in Commercial Distribution

  • 04046963451226 ()
GE464SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I+ D1.8MM
Aesculap AG
GE463SU
In Commercial Distribution

  • 04046963451202 ()
GE463SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I+ D1.0MM
Aesculap AG
GE461SU
In Commercial Distribution

  • 04046963451066 ()
GE461SU

  • Orthopaedic bur, single-use
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