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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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C-C Blade, Left 210mm, Ø22
K2M, INC.
8030-90015
In Commercial Distribution

  • 10888857553620 ()
8030-90015

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 190mm, Ø22
K2M, INC.
8030-90013
In Commercial Distribution

  • 10888857553606 ()
8030-90013

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 150mm, Ø22
K2M, INC.
8030-90009
In Commercial Distribution

  • 10888857553569 ()
8030-90009

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 140mm, Ø22
K2M, INC.
8030-90008
In Commercial Distribution

  • 10888857553552 ()
8030-90008

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 110mm, Ø22
K2M, INC.
8030-90005
In Commercial Distribution

  • 10888857553521 ()
8030-90005

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Left 80mm, Ø22
K2M, INC.
8030-90002
In Commercial Distribution

  • 10888857553491 ()
8030-90002

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 220mm, Ø22
K2M, INC.
8030-90031
In Commercial Distribution

  • 10888857553781 ()
8030-90031

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 210mm, Ø22
K2M, INC.
8030-90030
In Commercial Distribution

  • 10888857553774 ()
8030-90030

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 200mm, Ø22
K2M, INC.
8030-90029
In Commercial Distribution

  • 10888857553767 ()
8030-90029

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 190mm, Ø22
K2M, INC.
8030-90028
In Commercial Distribution

  • 10888857553750 ()
8030-90028

  • Surgical retractor/retraction system blade, reusable
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