SEARCH RESULTS FOR: 怎么做假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.DIAMOND BURR I D3.1MM
Aesculap AG
GE416SU
In Commercial Distribution

  • 04038653398645 ()
GE416SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.TWIST DRILL II D1.5MM
Aesculap AG
GE532SU
In Commercial Distribution

  • 04038653398638 ()
GE532SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D2.3MM
Aesculap AG
GE414SU
In Commercial Distribution

  • 04038653398614 ()
GE414SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D1.8MM
Aesculap AG
GE413SU
In Commercial Distribution

  • 04038653398591 ()
GE413SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR CRS.II D3.1MM
Aesculap AG
GE525SU
In Commercial Distribution

  • 04038653398584 ()
GE525SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAM.BURR CRS.II D2.3MM
Aesculap AG
GE524SU
In Commercial Distribution

  • 04038653398577 ()
GE524SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D1.4MM
Aesculap AG
GE412SU
In Commercial Distribution

  • 04038653398560 ()
GE412SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.LINDEMANN CUTTER II 20MM
Aesculap AG
GE523SU
In Commercial Distribution

  • 04038653398553 ()
GE523SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.LINDEMANN CUTTER II 12MM
Aesculap AG
GE522SU
In Commercial Distribution

  • 04038653398546 ()
GE522SU

  • Orthopaedic bur, single-use
HI-LINE XS DISP.DIAMOND BURR I D1.0MM
Aesculap AG
GE411SU
Not in Commercial Distribution

  • 04038653398539 ()
GE411SU

  • Orthopaedic bur, single-use
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