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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.
583858
In Commercial Distribution

  • 00886158004998 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583856
In Commercial Distribution

  • 00886158004974 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583850
In Commercial Distribution

  • 00886158004912 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583849
In Commercial Distribution

  • 00886158004905 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583848
In Commercial Distribution

  • 00886158004899 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583847
In Commercial Distribution

  • 00886158004882 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583846
In Commercial Distribution

  • 00886158004875 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583845
In Commercial Distribution

  • 00886158004868 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583844
In Commercial Distribution

  • 00886158004851 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583841
In Commercial Distribution

  • 00886158004820 ()


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