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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, Right 160mm, Ø22
K2M, INC.
8030-90025
In Commercial Distribution

  • 10888857553729 ()
8030-90025

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 90mm, Ø22
K2M, INC.
8030-90018
In Commercial Distribution

  • 10888857553651 ()
8030-90018

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

  • 10888857553781 ()
8030-90031

  • 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 150mm, Ø22
K2M, INC.
8030-90024
In Commercial Distribution

  • 10888857553712 ()
8030-90024

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 140mm, Ø22
K2M, INC.
8030-90023
In Commercial Distribution

  • 10888857553705 ()
8030-90023

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 130mm, Ø22
K2M, INC.
8030-90022
In Commercial Distribution

  • 10888857553699 ()
8030-90022

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 120mm, Ø22
K2M, INC.
8030-90021
In Commercial Distribution

  • 10888857553682 ()
8030-90021

  • Surgical retractor/retraction system blade, reusable
C-C Blade, Right 110mm, Ø22
K2M, INC.
8030-90020
In Commercial Distribution

  • 10888857553675 ()
8030-90020

  • Surgical retractor/retraction system blade, reusable
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