Company Name Brand Name GMDN Term FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class

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RHMK II 24W/12F
DIAGNOSTIC HYBRIDS, INC.
49-2412Y
In Commercial Distribution

  • 30014613332077 ()
49-2412Y

  • Cell culture line IVD
RHMK W24/12
DIAGNOSTIC HYBRIDS, INC.
49-2412A
In Commercial Distribution

  • 30014613332060 ()
49-2412A

  • Cell culture line IVD
RHMK W24/06
DIAGNOSTIC HYBRIDS, INC.
49-2406A
In Commercial Distribution

  • 30014613332053 ()
49-2406A

  • Cell culture line IVD
RHESUS II TUBE
DIAGNOSTIC HYBRIDS, INC.
49-0600Y
In Commercial Distribution

  • 30014613332046 ()
49-0600Y

  • Cell culture line IVD
RHMK TUBE W/ANTISER
DIAGNOSTIC HYBRIDS, INC.
49-0600A
In Commercial Distribution

  • 30014613332039 ()
49-0600A

  • Cell culture line IVD
RHMK TUBE
DIAGNOSTIC HYBRIDS, INC.
49-0600
In Commercial Distribution

  • 30014613332022 ()
49-0600

  • Cell culture line IVD
RHMK II SV W/C
DIAGNOSTIC HYBRIDS, INC.
49-0102Y
In Commercial Distribution

  • 30014613332015 ()
49-0102Y

  • Cell culture line IVD
RHMK SV W/C ANTISER
DIAGNOSTIC HYBRIDS, INC.
49-0102A
In Commercial Distribution

  • 30014613332008 ()
49-0102A

  • Cell culture line IVD
RHMK SV W/C
DIAGNOSTIC HYBRIDS, INC.
49-0102
In Commercial Distribution

  • 30014613331995 ()
49-0102

  • Cell culture line IVD
RHMK P1 FROZEN SUSP.
DIAGNOSTIC HYBRIDS, INC.
49-00010P
In Commercial Distribution

  • 30014613331988 ()
49-00010P

  • Cell culture line IVD
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