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 II D2.7MM
Aesculap AG
GE505SU
In Commercial Distribution

  • 04038653405619 ()
GE505SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR II D3.1MM
Aesculap AG
GE516SU
In Commercial Distribution

  • 04038653399208 ()
GE516SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR II D1.8MM
Aesculap AG
GE513SU
In Commercial Distribution

  • 04038653399185 ()
GE513SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR III D4.0MM
Aesculap AG
GE617SU
In Commercial Distribution

  • 04038653398904 ()
GE617SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR CRS.I D2.3MM
Aesculap AG
GE424SU
In Commercial Distribution

  • 04038653398898 ()
GE424SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR III D1.8MM
Aesculap AG
GE613SU
In Commercial Distribution

  • 04038653398850 ()
GE613SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR III D4.0MM
Aesculap AG
GE607SU
In Commercial Distribution

  • 04038653398829 ()
GE607SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR III D3.1MM
Aesculap AG
GE606SU
In Commercial Distribution

  • 04038653398812 ()
GE606SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.ROSEN BURR III D1.8MM
Aesculap AG
GE603SU
In Commercial Distribution

  • 04038653398782 ()
GE603SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.CRANIOTOME CUTTER I
Aesculap AG
GE420SU
In Commercial Distribution

  • 04038653398744 ()
GE420SU

  • Orthopaedic bur, single-use
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