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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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LAL, Sterile, Packaged, 25.0 Diopter
RXSIGHT, INC.
60005-2250
Not in Commercial Distribution

  • 00818806020265 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 22.5 Diopter
RXSIGHT, INC.
60005-2225
Not in Commercial Distribution

  • 00818806020227 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 21.5 Diopter
RXSIGHT, INC.
60005-2215
Not in Commercial Distribution

  • 00818806020203 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 21.0 Diopter
RXSIGHT, INC.
60005-2210
Not in Commercial Distribution

  • 00818806020197 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 20.5 Diopter
RXSIGHT, INC.
60005-2205
Not in Commercial Distribution

  • 00818806020180 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 20.0 Diopter
RXSIGHT, INC.
60005-2200
Not in Commercial Distribution

  • 00818806020173 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 19.5 Diopter
RXSIGHT, INC.
60005-2195
Not in Commercial Distribution

  • 00818806020166 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 19.0 Diopter
RXSIGHT, INC.
60005-2190
Not in Commercial Distribution

  • 00818806020159 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 18.5 Diopter
RXSIGHT, INC.
60005-2185
Not in Commercial Distribution

  • 00818806020142 ()


  • Posterior-chamber intraocular lens, pseudophakic
LAL, Sterile, Packaged, 18.0 Diopter
RXSIGHT, INC.
60005-2180
Not in Commercial Distribution

  • 00818806020135 ()


  • Posterior-chamber intraocular lens, pseudophakic
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