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 - 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

HI-LINE XS - 04038653398720

HI-LINE XS DISP.CONE BURR II D4.0MM
Aesculap AG
GE540SU
In Commercial Distribution

  • 04038653398720 ()
GE540SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398713

HI-LINE XS DISP.ACORN BURR II D6.0MM
Aesculap AG
GE537SU
In Commercial Distribution

  • 04038653398713 ()
GE537SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398706

HI-LINE XS DISP.DIAMOND BURR I D6.0MM
Aesculap AG
GE419SU
In Commercial Distribution

  • 04038653398706 ()
GE419SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398690

HI-LINE XS DISP.NEURO CUTTER II D3.1MM
Aesculap AG
GE535SU
In Commercial Distribution

  • 04038653398690 ()
GE535SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398683

HI-LINE XS DISP.DIAMOND BURR I D5.0MM
Aesculap AG
GE418SU
In Commercial Distribution

  • 04038653398683 ()
GE418SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398676

HI-LINE XS DISP.NEURO CUTTER II D2.3MM
Aesculap AG
GE534SU
In Commercial Distribution

  • 04038653398676 ()
GE534SU

  • Orthopaedic bur, single-use

HI-LINE XS - 04038653398669

HI-LINE XS DISP.DIAMOND BURR I D4.0MM
Aesculap AG
GE417SU
In Commercial Distribution

  • 04038653398669 ()
GE417SU

  • Orthopaedic bur, single-use
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