SEARCH RESULTS FOR: 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 - 04038653398850

HI-LINE XS DISP.DIAMOND BURR III D1.8MM
Aesculap AG
GE613SU
In Commercial Distribution

  • 04038653398850 ()
GE613SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398843

HI-LINE XS DISP.ROSEN BURR III D6.0MM
Aesculap AG
GE609SU
In Commercial Distribution

  • 04038653398843 ()
GE609SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398836

HI-LINE XS DISP.ROSEN BURR III D5.0MM
Aesculap AG
GE608SU
In Commercial Distribution

  • 04038653398836 ()
GE608SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398829

HI-LINE XS DISP.ROSEN BURR III D4.0MM
Aesculap AG
GE607SU
In Commercial Distribution

  • 04038653398829 ()
GE607SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398812

HI-LINE XS DISP.ROSEN BURR III D3.1MM
Aesculap AG
GE606SU
In Commercial Distribution

  • 04038653398812 ()
GE606SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398805

HI-LINE XS DISP.ROSEN BURR III D2.3MM
Aesculap AG
GE604SU
In Commercial Distribution

  • 04038653398805 ()
GE604SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398782

HI-LINE XS DISP.ROSEN BURR III D1.8MM
Aesculap AG
GE603SU
In Commercial Distribution

  • 04038653398782 ()
GE603SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398768

HI-LINE XS DISP.BARREL BURR II D6.0MM
Aesculap AG
GE546SU
In Commercial Distribution

  • 04038653398768 ()
GE546SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398744

HI-LINE XS DISP.CRANIOTOME CUTTER I
Aesculap AG
GE420SU
In Commercial Distribution

  • 04038653398744 ()
GE420SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398737

HI-LINE XS DISP.CONE BURR II D6.0MM
Aesculap AG
GE542SU
In Commercial Distribution

  • 04038653398737 ()
GE542SU

  • Orthopaedic bur, single-use
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