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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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CURVED LASER PROBE, 23G DORC
FCI S A S FCI 20 22
S9.1205.23
In Commercial Distribution

  • 23700773720334 ()
  • 13700773720337 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 23G NIDEK
FCI S A S FCI 20 22
S9.1204.23
In Commercial Distribution

  • 23700773720327 ()
  • 13700773720320 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 23G QUANTEL
FCI S A S FCI 20 22
S9.1203.23
In Commercial Distribution

  • 23700773720310 ()
  • 13700773720313 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 23G ALCON/COHERENT/ZEISS/ELLEX/OS4
FCI S A S FCI 20 22
S9.1202.23
In Commercial Distribution

  • 23700773720303 ()
  • 13700773720306 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 23G IRIDEX/B&L
FCI S A S FCI 20 22
S9.1201.23
In Commercial Distribution

  • 23700773720297 ()
  • 13700773720290 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 20G DORC
FCI S A S FCI 20 22
S9.1105.20
In Commercial Distribution

  • 23700773720280 ()
  • 13700773720283 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 20G NIDEK
FCI S A S FCI 20 22
S9.1104.20
In Commercial Distribution

  • 23700773720273 ()
  • 13700773720276 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 20G QUANTEL
FCI S A S FCI 20 22
S9.1103.20
In Commercial Distribution

  • 23700773720266 ()
  • 13700773720269 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 20G ALCON/COHERENT/ZEISS/ELLEX/OS4
FCI S A S FCI 20 22
S9.1102.20
In Commercial Distribution

  • 23700773720259 ()
  • 13700773720252 ()


  • Ophthalmic laser system beam guide
CURVED LASER PROBE, 20G IRIDEX/B&L
FCI S A S FCI 20 22
S9.1101.20
In Commercial Distribution

  • 23700773720242 ()
  • 13700773720245 ()


  • Ophthalmic laser system beam guide
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