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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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MONOAXIAL SCREW DRIVER
HYHTE HOLDINGS, INC.
NZA002008
In Commercial Distribution

  • 00840085257742 ()
NZA002008

  • Surgical screwdriver, reusable
NAVIGATED, HIGH TOP, SCREW DRIVER
HYHTE HOLDINGS, INC.
NZA002006
In Commercial Distribution

  • 00840085257728 ()
NZA002006

  • Surgical screwdriver, reusable
HIGH TOP SCREW DRIVER
HYHTE HOLDINGS, INC.
NZA002004
In Commercial Distribution

  • 00840085257704 ()
NZA002004

  • Surgical screwdriver, reusable
NAVIGATED, SCREW DRIVER
HYHTE HOLDINGS, INC.
NZA002002
In Commercial Distribution

  • 00840085257681 ()
NZA002002

  • Surgical screwdriver, reusable
SCREW DRIVER
HYHTE HOLDINGS, INC.
NZA002000
In Commercial Distribution

  • 00840085257667 ()
NZA002000

  • Surgical screwdriver, reusable
Set Screw Inserter, Long
ALPHATEC SPINE, INC.
19814
In Commercial Distribution

  • 00190376301877 ()


  • Surgical screwdriver, reusable
DRIVER CANNULATED 2MM
Smith & Nephew, Inc.
7207193
In Commercial Distribution

  • 03596010253491 ()
7207193

  • Orthopaedic implant driver
Reform® Ti Locking Polyaxial Driver
PRECISION SPINE, INC.
75-RT-0700
In Commercial Distribution

  • 00840019975711 ()
75-RT-0700

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reform® Ti Reduction Driver, Cannulated
PRECISION SPINE, INC.
70-RT-1730
In Commercial Distribution

  • 00840019975704 ()
70-RT-1730

  • Orthopaedic surgical procedure kit, non-medicated, reusable
Reform® MAX Modular Driver BOM (GLOBOT)
PRECISION SPINE, INC.
73-BK-0105
In Commercial Distribution

  • 00840019973076 ()
73-BK-0105

  • Neurosurgical retraction system, spinal
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