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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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IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 9
ARTHREX, INC.
AR-623-59
In Commercial Distribution

  • 00888867214767 ()
AR-623-59

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 8
ARTHREX, INC.
AR-623-58
In Commercial Distribution

  • 00888867214750 ()
AR-623-58

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 7
ARTHREX, INC.
AR-623-57
In Commercial Distribution

  • 00888867214743 ()
AR-623-57

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 6
ARTHREX, INC.
AR-623-56
In Commercial Distribution

  • 00888867214736 ()
AR-623-56

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 5
ARTHREX, INC.
AR-623-55
In Commercial Distribution

  • 00888867214729 ()
AR-623-55

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 4
ARTHREX, INC.
AR-623-54
In Commercial Distribution

  • 00888867214712 ()
AR-623-54

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 3
ARTHREX, INC.
AR-623-53
In Commercial Distribution

  • 00888867214705 ()
AR-623-53

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 2
ARTHREX, INC.
AR-623-52
In Commercial Distribution

  • 00888867214699 ()
AR-623-52

  • Surgical implant template, reusable
IBAL POROUS TKA,CUT BLK,4 IN 1,SZ 1
ARTHREX, INC.
AR-623-51
In Commercial Distribution

  • 00888867214682 ()
AR-623-51

  • Surgical implant template, reusable
MicroFrance® Belloc angled rasp, cutting in line, 190 mm
INTEGRA MICROFRANCE
CP975A
In Commercial Distribution

  • 10381780101208 ()
CP975A

  • Plastic surgery file/rasp
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