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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.
584913
In Commercial Distribution

  • 00886158008149 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584912
In Commercial Distribution

  • 00886158008132 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584911
In Commercial Distribution

  • 00886158008125 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584910
In Commercial Distribution

  • 00886158008118 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584906
In Commercial Distribution

  • 00886158008071 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584905
In Commercial Distribution

  • 00886158008064 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584904
In Commercial Distribution

  • 00886158008057 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584903
In Commercial Distribution

  • 00886158008040 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584902
In Commercial Distribution

  • 00886158008033 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584901
In Commercial Distribution

  • 00886158008026 ()


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