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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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MX60UET350 12.5MM +19.00
Bausch & Lomb Incorporated
MXUET350+190
In Commercial Distribution

  • 10757770556646 ()
MXUET350+190

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +18.50
Bausch & Lomb Incorporated
MXUET350+185
In Commercial Distribution

  • 10757770556639 ()
MXUET350+185

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +18.00
Bausch & Lomb Incorporated
MXUET350+180
In Commercial Distribution

  • 10757770556622 ()
MXUET350+180

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +17.50
Bausch & Lomb Incorporated
MXUET350+175
In Commercial Distribution

  • 10757770556615 ()
MXUET350+175

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +17.00
Bausch & Lomb Incorporated
MXUET350+170
In Commercial Distribution

  • 10757770556608 ()
MXUET350+170

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +16.50
Bausch & Lomb Incorporated
MXUET350+165
In Commercial Distribution

  • 10757770556592 ()
MXUET350+165

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +16.00
Bausch & Lomb Incorporated
MXUET350+160
In Commercial Distribution

  • 10757770556585 ()
MXUET350+160

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +15.50
Bausch & Lomb Incorporated
MXUET350+155
In Commercial Distribution

  • 10757770556578 ()
MXUET350+155

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +15.00
Bausch & Lomb Incorporated
MXUET350+150
In Commercial Distribution

  • 10757770556561 ()
MXUET350+150

  • Posterior-chamber intraocular lens, pseudophakic
MX60UET350 12.5MM +14.50
Bausch & Lomb Incorporated
MXUET350+145
In Commercial Distribution

  • 10757770556554 ()
MXUET350+145

  • Posterior-chamber intraocular lens, pseudophakic
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