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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.
584815
In Commercial Distribution

  • 00886158007111 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584814
In Commercial Distribution

  • 00886158007081 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584813
In Commercial Distribution

  • 00886158007074 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584812
In Commercial Distribution

  • 00886158007067 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584811
In Commercial Distribution

  • 00886158007050 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584810
In Commercial Distribution

  • 00886158007029 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584808
In Commercial Distribution

  • 00886158007005 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584807
In Commercial Distribution

  • 00886158006992 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584805
In Commercial Distribution

  • 00886158006978 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584801
In Commercial Distribution

  • 00886158006930 ()


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