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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.
583913
In Commercial Distribution

  • 00886158005773 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583910
In Commercial Distribution

  • 00886158005742 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583908
In Commercial Distribution

  • 00886158005728 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583906
In Commercial Distribution

  • 00886158005582 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583898
In Commercial Distribution

  • 00886158005483 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583895
In Commercial Distribution

  • 00886158005445 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583893
In Commercial Distribution

  • 00886158005421 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583889
In Commercial Distribution

  • 00886158005346 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583887
In Commercial Distribution

  • 00886158005322 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
583885
In Commercial Distribution

  • 00886158005308 ()


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