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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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Venue Fit R4 MD physical
GE MEDICAL SYSTEMS, ULTRASOUND & PRIMARY CARE DIAGNOSTICS, LLC
R4 UPG
In Commercial Distribution

  • 00195278513014 ()


  • General-purpose ultrasound imaging system
Voluson P6 BT22
GE Ultrasound Korea Ltd.
P6 BT22
In Commercial Distribution

  • 00195278473097 ()
VOLUSON-P6-BT22

  • General-purpose ultrasound imaging system
Voluson S8 BT22
GE Ultrasound Korea Ltd.
S8 BT22
In Commercial Distribution

  • 00195278473073 ()
VOLUSON-S8-BT22

  • General-purpose ultrasound imaging system
Voluson S8t BT22
GE Ultrasound Korea Ltd.
S8t BT22
In Commercial Distribution

  • 00195278473066 ()
VOLUSON-S8t-BT22

  • General-purpose ultrasound imaging system
Voluson S10 Expert BT22
GE Ultrasound Korea Ltd.
S10 Expert BT22
In Commercial Distribution

  • 00195278473042 ()
VOLUSON-S10Expert-BT22

  • General-purpose ultrasound imaging system
Voluson Performance to BT22 UPG
GE Ultrasound Korea Ltd.
Performance to BT22 UPG
In Commercial Distribution

  • 00195278473011 ()
Voluson-Performance-to-BT22-UPG

  • General-purpose ultrasound imaging system
LOGIQ P10 R4.5 HD
GE Ultrasound Korea Ltd.
P10 R4.5 HD
In Commercial Distribution

  • 00195278464668 ()


  • General-purpose ultrasound imaging system
LP10 R4 to R4.5 SW Conversion
GE Ultrasound Korea Ltd.
P10 R4 to R4.5 SW Conversion
In Commercial Distribution

  • 00195278464620 ()


  • General-purpose ultrasound imaging system
LOGIQ Fortis HDU Console
GE Ultrasound Korea Ltd.
FORTIS HDU
In Commercial Distribution

  • 00195278405326 ()


  • General-purpose ultrasound imaging system
Voluson Expert 22
GE Healthcare Austria GmbH & Co OG
Expert 22
In Commercial Distribution

  • 00195278347497 ()


  • General-purpose ultrasound imaging system
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