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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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Readypak Kit
Beaver-Visitec International, Inc.
584135
In Commercial Distribution

  • 00886158003724 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584134
In Commercial Distribution

  • 00886158003717 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584128
In Commercial Distribution

  • 00886158003670 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584117
In Commercial Distribution

  • 00886158003663 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
EYE PACK
Cardinal Health 200, LLC
SEY31CAPC3
In Commercial Distribution

  • 50197106068357 ()
  • 10197106068359 ()
SEY31CAPC3

  • Ophthalmic surgical procedure kit, non-medicated, single-use
EYE PACK
Cardinal Health 200, LLC
SEY69EPKO4
In Commercial Distribution

  • 50197106068272 ()
  • 10197106068274 ()
SEY69EPKO4

  • Ophthalmic surgical procedure kit, non-medicated, single-use
EYE TRAY PACK
Cardinal Health 200, LLC
SEY19EYKH5
In Commercial Distribution

  • 50197106067930 ()
  • 10197106067932 ()
SEY19EYKH5

  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583821
In Commercial Distribution

  • 00886158012030 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
CustomEyes Kit
Beaver-Visitec International, Inc.
58000042
In Commercial Distribution

  • 00886158008668 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584947
In Commercial Distribution

  • 00886158008613 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
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