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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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In Situ Bender, Right
PRECISION SPINE, INC.
59-RD-0051
In Commercial Distribution

  • 00840019927727 ()
59-RD-0051

  • Orthopaedic surgical procedure kit, non-medicated, reusable
In Situ Bender, Left
PRECISION SPINE, INC.
59-RD-0050
In Commercial Distribution

  • 00840019927710 ()
59-RD-0050

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Sleeve, All in One
PRECISION SPINE, INC.
48-9001
In Commercial Distribution

  • 00840019922517 ()
48-9001

  • Orthopaedic surgical procedure kit, non-medicated, reusable
LEFT IN SITU BENDER
MEDICREA INTERNATIONAL
A01170602
Not in Commercial Distribution

  • 03613720210801 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
RIGHT IN SITU BENDER
MEDICREA INTERNATIONAL
A01170601
Not in Commercial Distribution

  • 03613720210795 ()


  • Orthopaedic surgical procedure kit, non-medicated, reusable
ABBEY NH 5 IN
SKLAR CORPORATION
97-894
In Commercial Distribution

  • 10649111239595 ()


  • Suturing needle holder, reusable
In situ Poly inserter
Ascension Orthopedics, Inc.
MJU940T
In Commercial Distribution

  • 10381780368878 ()


  • Joint prosthesis implantation kit, reusable
T-25 In Situ Driver
NEXXT SPINE, LLC
I20-10-02
In Commercial Distribution

  • 00889929050293 ()


  • General internal orthopaedic fixation system implantation kit
In Situ Bender, Right
GLOBUS MEDICAL, INC.
602.511
In Commercial Distribution

  • 00889095139846 ()


  • Manual orthopaedic bender, reusable
In Situ Bender, Left
GLOBUS MEDICAL, INC.
602.510
In Commercial Distribution

  • 00889095139839 ()


  • Manual orthopaedic bender, reusable
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