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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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Lordotic Trial D12 H11
SpineArt SA
TRY-IL 12 06-N
In Commercial Distribution

  • 07640151081539 ()
TRY-IL 12 06-N

  • Surgical implant/trial-implant/sizer holder, reusable
Lordotic Trial D12 H05
SpineArt SA
TRY-IL 12 05-N
In Commercial Distribution

  • 07640151081522 ()
TRY-IL 12 05-N

  • Surgical implant/trial-implant/sizer holder, reusable
Curette
SpineArt SA
PAD-IN 08 00-N
In Commercial Distribution

  • 07640151081508 ()
PAD-IN 08 00-N

  • Bone curette, reusable
PERCUTANEOUS ROD HOLDER
SpineArt SA
MIS-IN 40 01-N
In Commercial Distribution

  • 07640151080686 ()
MIS-IN 40 01-N

  • Surgical implant/trial-implant/sizer holder, reusable
No Description
Lake Region Medical
LR1BR003
In Commercial Distribution

  • 00816349011320 ()

  • Outer Diameter: 5.4 Femtometer
  • Length: 105 Centimeter


  • Endomyocardial biopsy forceps, single-use
No Description
Lake Region Medical
LR1BR001
In Commercial Distribution

  • 00816349011313 ()

  • Outer Diameter: 5.4 Femtometer
  • Length: 50 Centimeter


  • Endomyocardial biopsy forceps, single-use
Rod Rocker
BACK 2 BASIC DIRECT, LLC
06.0
In Commercial Distribution

  • 00815500025480 ()
09.0722

  • Surgical implant/trial-implant/sizer holder, reusable
Rod forceps 5.5mm
BACK 2 BASIC DIRECT, LLC
06.0
In Commercial Distribution

  • 00815500025299 ()
09.0665

  • Surgical implant/trial-implant/sizer holder, reusable
Rod Gripper - 5.5mm
BACK 2 BASIC DIRECT, LLC
06.0
In Commercial Distribution

  • 00815500025244 ()
77.2048

  • Surgical implant/trial-implant/sizer holder, reusable
Implant Holder
SpineArt SA
PAD-IN 03 00-N
In Commercial Distribution

  • 07640139349286 ()
PAD-IN 03 00-N

  • Surgical implant/trial-implant/sizer holder, reusable
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