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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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SOFT PLUG® Silicone Punctum Plug, Small (0.7 mm), Pen-Style Inserter
OASIS MEDICAL, INC.
7713-FC
In Commercial Distribution

  • 10845819006419 ()
  • 00845819006412 ()


  • Lacrimal punctum plug
SOFT PLUG® Silicone Punctum Plug, Petite (0.6 mm), Pen-Style Inserter
OASIS MEDICAL, INC.
7712-FC
In Commercial Distribution

  • 10845819006402 ()
  • 00845819006405 ()


  • Lacrimal punctum plug
Lacrimal Irrigation Kit, 3-mL Disposable Syringe and a 25g x 1-1/8", Blunt Disposable Cannula
OASIS MEDICAL, INC.
4003-IK
In Commercial Distribution

  • 10845819006099 ()
  • 00845819006092 ()


  • Lacrimal intubation set
SCREW X0410304 CORT NON-CANN TI 4.0X24
MEDTRONIC SOFAMOR DANEK, INC.
X0410304
In Commercial Distribution

  • 00613994799623 ()

  • Length: 24.0 Millimeter
  • Outer Diameter: 4.0 Millimeter


  • Spinal bone screw, non-bioabsorbable
SCREW X0410303 CORT NON-CANN TI 4.0X22
MEDTRONIC SOFAMOR DANEK, INC.
X0410303
In Commercial Distribution

  • 00613994799616 ()

  • Length: 22.0 Millimeter
  • Outer Diameter: 4.0 Millimeter


  • Spinal bone screw, non-bioabsorbable
SCREW X0410169 CORT NON-CANN TI 3.5X10
MEDTRONIC SOFAMOR DANEK, INC.
X0410169
In Commercial Distribution

  • 00613994799555 ()

  • Outer Diameter: 3.5 Millimeter
  • Length: 10.0 Millimeter


  • Spinal bone screw, non-bioabsorbable
PrimaLOK FF 3mm Cannulated Power Drill
OSTEOMED LLC
800-1221
Not in Commercial Distribution

  • 00845694037730 ()
800-1221

  • General internal orthopaedic fixation system implantation kit
PrimaLOK FF EMG Cannula
OSTEOMED LLC
800-1206
Not in Commercial Distribution

  • 00845694037686 ()
800-1206

  • General internal orthopaedic fixation system implantation kit
PrimaLOK FF Standard Cannula
OSTEOMED LLC
800-1205
Not in Commercial Distribution

  • 00845694037679 ()
800-1205

  • General internal orthopaedic fixation system implantation kit
PrimaLOK FF Guide Wire Stiffener
OSTEOMED LLC
800-1204
Not in Commercial Distribution

  • 00845694037662 ()
800-1204

  • General internal orthopaedic fixation system implantation kit
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