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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No Description
Bonebridge AG
B-420012
In Commercial Distribution

  • 07640187461565 ()


  • Surgical instrument/implant rack
No Description
Bonebridge AG
B-410008
In Commercial Distribution

  • 07640187460636 ()


  • Surgical instrument/implant rack
TRAY FOR NON STERILE IMPLANTS
SpineArt SA
MOS-BX 23 01-N
In Commercial Distribution

  • 07640178989863 ()
MOS-BX 23 01-N

  • Surgical instrument/implant rack
TRAY FOR NON STERILE IMPLANTS
SpineArt SA
MOS-BX 22 01-N
In Commercial Distribution

  • 07640178989832 ()
MOS-BX 22 01-N

  • Surgical instrument/implant rack
TRAY FOR NON STERILE IMPLANTS
SpineArt SA
MOS-BX 21 01-N
In Commercial Distribution

  • 07640178989818 ()
MOS-BX 21 01-N

  • Surgical instrument/implant rack
LC IMPLANT BOX
SpineArt SA
ROM-BX 21 01-N
In Commercial Distribution

  • 07640178989405 ()
ROM-BX 21 01-N

  • Surgical instrument/implant rack
IMPLANT BOX
SpineArt SA
ROM-BX 20 01-N
In Commercial Distribution

  • 07640178989399 ()
ROM-BX 20 01-N

  • Surgical instrument/implant rack
EMPTY TRAY FOR NON STERILE IMPLANTS
SpineArt SA
ELL-BX 20 00-N
In Commercial Distribution

  • 07640178989320 ()
ELL-BX 20 00-N

  • Surgical instrument/implant rack
TRAY FOR NON STERILE IMPLANTS (JULIET ® TL)
SpineArt SA
DYN-BX 23 01-N
In Commercial Distribution

  • 07640178989085 ()
DYN-BX 23 01-N

  • Surgical instrument/implant rack
TRAY FOR NON STERILE IMPLANTS (JULIET ® PO)
SpineArt SA
DYN-BX 21 01-N
In Commercial Distribution

  • 07640178989054 ()
DYN-BX 21 01-N

  • Surgical instrument/implant rack
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