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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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Screwdrivers 1.0mm Hex, 34mm Length
DIAMODENT INC
N/A
In Commercial Distribution

  • D907T51170 ()
T5117

  • Surgical screwdriver, reusable
Screwdrivers 1.0mm Hex, 21mm Length
DIAMODENT INC
N/A
In Commercial Distribution

  • D907T51150 ()
T5115

  • Surgical screwdriver, reusable
Screwdrivers 1.0mm Hex, 28.2mm Length
DIAMODENT INC
N/A
In Commercial Distribution

  • D907T51100 ()
T5110

  • Surgical screwdriver, reusable
Screwdrivers .35" Hex, 21mm Length
DIAMODENT INC
N/A
In Commercial Distribution

  • D907T51050 ()
T5105

  • Surgical screwdriver, reusable
Screwdrivers .35" Hex, 28.2mm Length
DIAMODENT INC
N/A
In Commercial Distribution

  • D907T51000 ()
T5100

  • Surgical screwdriver, reusable
Internal Thread Tap Standard
AMERICAN DENTAL IMPLANT CORPORATION
ITTS
In Commercial Distribution

  • D896ITTS0 ()
ITTS

  • Surgical screwdriver, reusable
Provisional Split Driver Size 30 Small Handle
K2M, INC.
5101-90193
In Commercial Distribution

  • 10888857290662 ()
5101-90193

  • Orthopaedic implant driver
Driver Sleeve
K2M, INC.
5101-90186
In Commercial Distribution

  • 10888857283428 ()
5101-90186

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Lordosis/Kyphosis Driver Inner Shaft, Size Inner Shaft
K2M, INC.
2112-90053
In Commercial Distribution

  • 10888857279209 ()
2112-90053

  • Orthopaedic prosthesis implantation positioning instrument, reusable
Lordosis/Kyphosis Driver Outer Shaft, Size Outer Shaft
K2M, INC.
2112-90052
In Commercial Distribution

  • 10888857279148 ()
2112-90052

  • Orthopaedic prosthesis implantation positioning instrument, reusable
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