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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5720-10-025 STRYKER QUANTUM DRL RFB 6
MEDLINE INDUSTRIES, INC.
572010025RH
In Commercial Distribution

  • 10888277404700 ()
572010025RH

  • Arthroscopic shaver system blade, reprocessed
5720-10-020 STRYKER QUANTUM DRL RFB 6
MEDLINE INDUSTRIES, INC.
572010020RH
In Commercial Distribution

  • 10888277404694 ()
572010020RH

  • Arthroscopic shaver system blade, reprocessed
5720-10-015 STRYKER QUANTUM DRL RFB 6
MEDLINE INDUSTRIES, INC.
572010015RH
In Commercial Distribution

  • 10888277404687 ()
572010015RH

  • Arthroscopic shaver system blade, reprocessed
5720-10-010 STRYKER QUANTUM DRL RFBS 6
MEDLINE INDUSTRIES, INC.
572010010RH
In Commercial Distribution

  • 10888277404670 ()
572010010RH

  • Arthroscopic shaver system blade, reprocessed
5720-10-005 STRYKER QUANTUM DRL RFBS 4
MEDLINE INDUSTRIES, INC.
572010005RH
In Commercial Distribution

  • 10888277404663 ()
572010005RH

  • Arthroscopic shaver system blade, reprocessed
Quantum AdapterLight Handle Cover With Flange
DEROYAL INDUSTRIES, INC.
AM2-F
In Commercial Distribution

  • 50749756955190 ()
  • 00749756955195 ()


  • Instrument/equipment drape, single-use, sterile
Vacuum Infiltration Processor, 230 VAC, 50/60 Hz, 6.0 Amps
SAKURA FINETEK U.S.A., INC.
6042
In Commercial Distribution

  • 04946433600584 ()


  • Tissue processor IVD, automated/semi-automated
Novaloc® Equipment Box with 3 Instruments, PP / PS / stainless steel / AI
Institut Straumann AG
Non-invasive Instruments
In Commercial Distribution

  • 07630031759061 ()
2010.101-NOV

  • Dental precision attachment fitting/adjustment tool
Optiloc® Equipment Box with 3 Instruments, PP / PS / stainless steel / AI
Institut Straumann AG
Non-invasive Instruments
In Commercial Distribution

  • 07630031759054 ()
5102.0000-OPT

  • Dental precision attachment fitting/adjustment tool
Validate LP2 is intended for the quantitative determination of Calibration Verification/Linearity on automated instruments.
Lgc Clinical Diagnostics, Inc.
507ro
In Commercial Distribution

  • 00859110005869 ()

  • 2 tests
507ro

  • Apolipoprotein A-I (Apo A1) IVD, control
  • Apolipoprotein B (Apo B) IVD, control
  • Multiple lipid analyte IVD, control
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