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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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Sklar® - 10649111090462

RUSH AWL & REAMER 3.2MM 8 1/4"
SKLAR CORPORATION
40-1637
In Commercial Distribution

  • 10649111090462 ()


  • Bone awl, reusable

Sklar® - 10649111090257

RUSH AWL & REAMER 2.4MM 7 1/2"
SKLAR CORPORATION
40-1636
In Commercial Distribution

  • 10649111090257 ()


  • Bone awl, reusable

Sklar® - 10649111089886

SHOULDER PERCUSSION AWL CVD 9"
SKLAR CORPORATION
40-1634
In Commercial Distribution

  • 10649111089886 ()


  • Bone awl, reusable

Sklar® - 10649111089688

SHOULDER PERCUSSION AWL CVD 7"
SKLAR CORPORATION
40-1633
In Commercial Distribution

  • 10649111089688 ()


  • Bone awl, reusable

Sklar® - 10649111089275

SHOULDER PERCUSSION AWL M 8.5
SKLAR CORPORATION
40-1631
In Commercial Distribution

  • 10649111089275 ()


  • Bone awl, reusable

ROMEO 2 MIS - 07640178985018

Trocar awl
SpineArt SA
MIS-IN 52 13-N
In Commercial Distribution

  • 07640178985018 ()


  • Bone awl, reusable

ROMEO 2 MIS - 07640178985001

Trocar needle
SpineArt SA
MIS-IN 52 12-N
In Commercial Distribution

  • 07640178985001 ()


  • Bone awl, reusable

ROMEO 2 MIS - 07640178984998

Needle cap
SpineArt SA
MIS-IN 52 11-N
In Commercial Distribution

  • 07640178984998 ()


  • Bone awl, reusable

ROMEO 2 MIS - 07640178984981

Trocar Handle
SpineArt SA
MIS-IN 52 10-N
In Commercial Distribution

  • 07640178984981 ()


  • Bone awl, reusable

ROMEO 2 INSTRUMENTATION - 07640178981959

PEDICLE PROBE LENKE STRAIGHT
SpineArt SA
ELL-IN 02 26-N
In Commercial Distribution

  • 07640178981959 ()
ELL-IN 02 26-N

  • Bone awl, reusable
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