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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.
583834
In Commercial Distribution

  • 00886158004752 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583833
In Commercial Distribution

  • 00886158004745 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583832
In Commercial Distribution

  • 00886158004738 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583831
In Commercial Distribution

  • 00886158004721 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583830
In Commercial Distribution

  • 00886158004714 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583829
In Commercial Distribution

  • 00886158004707 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583828
In Commercial Distribution

  • 00886158004691 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584827
In Commercial Distribution

  • 00886158004639 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584826
In Commercial Distribution

  • 00886158004622 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583825
In Commercial Distribution

  • 00886158004615 ()


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