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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ELAN 4 - 04046964726019

ELAN 4 MIS L10 DISP.ROSEN BURR D3.0
Aesculap AG
GP422SU
In Commercial Distribution

  • 04046964726019 ()
GP422SU

  • Orthopaedic bur, single-use

ELAN 4 - 04046964726002

ELAN 4 MIS L13 DISP.NEURO CUTTER D3.0
Aesculap AG
GP441SU
In Commercial Distribution

  • 04046964726002 ()
GP441SU

  • Orthopaedic bur, single-use

ELAN 4 - 04046964725999

ELAN 4 MIS L13 DISP.DIAMOND BURR D4.0
Aesculap AG
GP453SU
In Commercial Distribution

  • 04046964725999 ()
GP453SU

  • Orthopaedic bur, single-use

ELAN 4 - 04046964725982

ELAN 4 MIS L10 DISP.DIAMOND BURR D4.0
Aesculap AG
GP433SU
In Commercial Distribution

  • 04046964725982 ()
GP433SU

  • Orthopaedic bur, single-use

ELAN 4 - 04046964725968

ELAN 4 MIS L10 DISP.DIAMOND BURR D3.0
Aesculap AG
GP432SU
In Commercial Distribution

  • 04046964725968 ()
GP432SU

  • Orthopaedic bur, single-use

ELAN 4 - 04046964725944

ELAN 4 MIS L10 NEURO CUTT.DIAM.XCRS D5.0
Aesculap AG
GP430SU
In Commercial Distribution

  • 04046964725944 ()
GP430SU

  • Orthopaedic bur, single-use

ELAN 4 - 04046964725920

ELAN 4 MIS L10 DISP.NEURO CUTTER D3.0
Aesculap AG
GP421SU
In Commercial Distribution

  • 04046964725920 ()
GP421SU

  • Orthopaedic bur, single-use

AESCULAP - 04046964076800

HI-LINE XXS DISP.DIAMOND BURR III D5.0MM
Aesculap AG
GE848SU
In Commercial Distribution

  • 04046964076800 ()
GE848SU

  • Orthopaedic bur, single-use

AESCULAP - 04046964076695

HI-LINE XXS DIAM.NEURO CUTTER III D2.0MM
Aesculap AG
GE842SU
In Commercial Distribution

  • 04046964076695 ()
GE842SU

  • Orthopaedic bur, single-use

AESCULAP - 04046964076688

HI-LINE XXS DISP.ROSEN BURR III D4.0MM
Aesculap AG
GE835SU
In Commercial Distribution

  • 04046964076688 ()
GE835SU

  • Orthopaedic bur, single-use
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