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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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Laser Probe, straight, with DORC connector 20 gauge / 0.9mm - 08717872013992

No Description
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
7011.DORC
In Commercial Distribution

  • 08717872013992 ()
  • 18717872013999 ()
7011.DORC

  • Ophthalmic laser system beam guide

Laser probe, curved, with DORC connector 20 gauge / 0.9mm - 08717872013954

No Description
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
7010.DORC
In Commercial Distribution

  • 08717872013954 ()
  • 18717872013951 ()
7010.DORC

  • Ophthalmic laser system beam guide

Directional Laser Probe with DORC connector.(20 gauge / 0.9 mm) - 08717872014975

No Description
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
7220.DORC
In Commercial Distribution

  • 18717872014972 ()
  • 08717872014975 ()


  • Ophthalmic laser system beam guide

25-27G BriteLight™ Angled 20° EndoProbe® Box of 6 - 00813125015725

No Description
IRIDEX CORPORATION
14560
In Commercial Distribution

  • 00813125015725 ()


  • Ophthalmic laser system beam guide

Directional Laser Probe with Alcon / Lumenis connector.(20 gauge / 0.9 mm) - 08717872014142

No Description
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
7220.ALC
In Commercial Distribution

  • 18717872014149 ()
  • 08717872014142 ()


  • Ophthalmic laser system beam guide

Acculite EndoOto - 07290109140834

No Description
LUMENIS INC.
Horn, 24ga 20° Angled, SMA 906, 200µm
Not in Commercial Distribution

  • 17290109140831 ()
  • 07290109140834 ()


  • Ophthalmic laser system beam guide

Acculite EndoOcular - 07290109140742

No Description
LUMENIS INC.
Standard, 20ga 20° bend, SMA 906, 200µm
Not in Commercial Distribution

  • 07290109140742 ()
  • 17290109140749 ()


  • Ophthalmic laser system beam guide
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