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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SUPER E-MIX CELLS MWP W48/06F
DIAGNOSTIC HYBRIDS, INC.
92-4806
In Commercial Distribution

  • 30014613334705 ()
92-4806

  • Cell culture line IVD
SUPER E-MIX CELLS MWP W24/24F
DIAGNOSTIC HYBRIDS, INC.
92-2424S
In Commercial Distribution

  • 30014613334699 ()
92-2424S

  • Cell culture line IVD
SUPER E-MIX CELLS MWP W24/24F
DIAGNOSTIC HYBRIDS, INC.
92-2424
In Commercial Distribution

  • 30014613334682 ()
92-2424

  • Cell culture line IVD
SUPER E-MIX CELLS MWP W24/18F
DIAGNOSTIC HYBRIDS, INC.
92-2418
In Commercial Distribution

  • 30014613334675 ()
92-2418

  • Cell culture line IVD
SUPER E-MIX MWP W24/12F W/CS
DIAGNOSTIC HYBRIDS, INC.
92-2412S
In Commercial Distribution

  • 30014613334668 ()
92-2412S

  • Cell culture line IVD
SUPER E-MIX CELLS MWP W24/12F
DIAGNOSTIC HYBRIDS, INC.
92-2412
In Commercial Distribution

  • 30014613334651 ()
92-2412

  • Cell culture line IVD
SUPER E-MIX 24W/8F CUSTOM
DIAGNOSTIC HYBRIDS, INC.
92-2408CN
In Commercial Distribution

  • 30014613334644 ()
92-2408CN

  • Cell culture line IVD
SUPER E-MIX 24W/6F
DIAGNOSTIC HYBRIDS, INC.
92-2406
In Commercial Distribution

  • 30014613334637 ()
92-2406

  • Cell culture line IVD
SUPER E-MIX CLUST PLT 6W/6F
DIAGNOSTIC HYBRIDS, INC.
92-0606
In Commercial Distribution

  • 30014613334620 ()
92-0606

  • Cell culture line IVD
SUPER E-MIX SV/CS
DIAGNOSTIC HYBRIDS, INC.
92-0102
In Commercial Distribution

  • 30014613334613 ()
92-0102

  • Cell culture line IVD
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