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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Artisan Myopia 5/8.5mm -14.0D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060515 ()

  • -14.0 Power, D
206US1W28N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -13.5D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060508 ()

  • -13.5 Power, D
206US1W27N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -13.0D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060492 ()

  • -13.0 Power, D
206US1W26N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -12.5D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060485 ()

  • -12.5 Power, D
206US1W25N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -12.0D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060478 ()

  • -12.0 Power, D
206US1W24N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -11.5D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060461 ()

  • -11.5 Power, D
206US1W23N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -11.0D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060454 ()

  • -11.0 Power, D
206US1W22N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -10.0D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060430 ()

  • -10.0 Power, D
206US1W20N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -8.5D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060409 ()

  • -8.5 Power, D
206US1W17N

  • Anterior-chamber intraocular lens, phakic
Artisan Myopia 5/8.5mm -7.5D
Ophtec B.V.
206US1W
In Commercial Distribution

  • 08717819060386 ()

  • -7.5 Power, D
206US1W15N

  • Anterior-chamber intraocular lens, phakic
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