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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 Device Size Type Device Class Implantable

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ORTHO CLINIC MSR PACK
Cardinal Health 200, LLC
SOP73COKS5
In Commercial Distribution

  • 50197106896868 ()
  • 10197106896860 ()
SOP73COKS5

  • Orthopaedic surgical procedure kit, medicated
ORTHO CLINIC MSR PACK
Cardinal Health 200, LLC
SOP73COKS3
In Commercial Distribution

  • 50197106607273 ()
  • 10197106607275 ()
SOP73COKS3

  • Orthopaedic surgical procedure kit, medicated
ORTHO CLINIC MSR PACK
Cardinal Health 200, LLC
SOP73COKS4
In Commercial Distribution

  • 50197106632602 ()
  • 10197106632604 ()
SOP73COKS4

  • Orthopaedic surgical procedure kit, medicated
ORTHO CLINIC MSR PACK
Cardinal Health 200, LLC
SOP73COKSA
In Commercial Distribution

  • 50195594396471 ()
  • 10195594396473 ()
SOP73COKSA

  • Orthopaedic surgical procedure kit, medicated
ORTHO CLINIC MSR PACK
Cardinal Health 200, LLC
SOP73COKS1
In Commercial Distribution

  • 50195594628152 ()
  • 10195594628154 ()
SOP73COKS1

  • Orthopaedic surgical procedure kit, medicated
INSTRUMENT 8691015 CRSLK MSR TOOL CRD17
MEDTRONIC SOFAMOR DANEK, INC.
8691015
In Commercial Distribution

  • 00681490902922 ()


  • Bone-screw internal spinal fixation system connector
INSTRUMENT 8691013 CRSLK MSR TOOL CRD13
MEDTRONIC SOFAMOR DANEK, INC.
8691013
In Commercial Distribution

  • 00681490902908 ()


  • Bone-screw internal spinal fixation system connector
INSTRUMENT 8691012 CRSLK MSR TOOL CRD11
MEDTRONIC SOFAMOR DANEK, INC.
8691012
In Commercial Distribution

  • 00681490902892 ()


  • Bone-screw internal spinal fixation system connector
The Coxiella burnetii (Q-Fever) Phase 1 IgG ELISA is intended for the qualitative determination of IgG class antibodies against Coxiella burnetii (Q-Fever) Phase 1 in human serum or plasma (citrate, heparin).
DRG Instruments Gesellschaft mit beschränkter Haftung
EIA-5188
Not in Commercial Distribution

  • 00404847451887 ()
EIA-5188

  • Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
The Coxiella burnetii (Q-Fever) Phase 2 IgG ELISA is intended for the qualitative determination of IgG class antibodies against Coxiella burnetii (Q-Fever) Phase 2 in human serum or plasma (citrate, heparin).
DRG Instruments Gesellschaft mit beschränkter Haftung
EIA-5189
Not in Commercial Distribution

  • 00404847451894 ()
EIA-5189

  • Coxiella burnetii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
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