SEARCH RESULTS FOR: 仿制AT(5634 results)

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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.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
HI-LINE XS DISP.TWIST DRILL/GB740R D1.0
Aesculap AG
GE390SU
In Commercial Distribution

  • 04038653463367 ()
GE390SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR/GB740R D6.0
Aesculap AG
GE399SU
Not in Commercial Distribution

  • 04038653463343 ()
GE399SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TWINCUT BURR/GB740R D6.0
Aesculap AG
GE397SU
Not in Commercial Distribution

  • 04038653463329 ()
GE397SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR/GB740R D5.0
Aesculap AG
GE398SU
In Commercial Distribution

  • 04038653463305 ()
GE398SU

  • Orthopaedic bur, single-use
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