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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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CustomEyes Kit
Beaver-Visitec International, Inc.
58000042
In Commercial Distribution

  • 00886158008668 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584947
In Commercial Distribution

  • 00886158008613 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584931
In Commercial Distribution

  • 00886158008385 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584930
In Commercial Distribution

  • 00886158008378 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584929
In Commercial Distribution

  • 00886158008361 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584928
In Commercial Distribution

  • 00886158008347 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584927
In Commercial Distribution

  • 00886158008330 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584926
In Commercial Distribution

  • 00886158008323 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584925
In Commercial Distribution

  • 00886158008316 ()


  • Ophthalmic surgical procedure kit, non-medicated, single-use
Readypak Kit
Beaver-Visitec International, Inc.
584923
In Commercial Distribution

  • 00886158008293 ()


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