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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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NA - 00841983103728

CABLE ASSEMBLY, PHOTIC, 3 FT
NIHON KOHDEN AMERICA, INC.
A/PHOTIC-3
In Commercial Distribution

  • 00841983103728 ()
A/PHOTIC-3

  • General-purpose multi-parameter bedside monitor

NA - 00841983103711

HL-7 NEUROWORKBENCH INTERFACE
NIHON KOHDEN AMERICA, INC.
A/NWB-HL7NIS
In Commercial Distribution

  • 00841983103711 ()
A/NWB-HL7NIS

  • Medical networking interface unit

MODO - 00841983103704

CART FOR EEG-9200 / EEG-1200
NIHON KOHDEN AMERICA, INC.
A/NIH8000
In Commercial Distribution

  • 00841983103704 ()
A/NIH8000

  • Instrument trolley

GCX - 00841983103698

VHRS EEG CART WITHOUT CAMERA
NIHON KOHDEN AMERICA, INC.
A/GCXCART
In Commercial Distribution

  • 00841983103698 ()
A/GCXCART

  • Instrument trolley

NA - 00841983103681

DC INPUT BOX FOR JE-120A AMPLIFIER
NIHON KOHDEN AMERICA, INC.
A/DCIN1200
In Commercial Distribution

  • 00841983103681 ()
A/DCIN1200

  • Electroencephalograph

EEG Trend Program - 00841983103674

EEG TREND SOFTWARE REVIEW, 10 USER
NIHON KOHDEN AMERICA, INC.
QP-160R-10
In Commercial Distribution

  • 00841983103674 ()
QP-160R-10

  • Electroencephalograph

NEUROFAX - 00841983103650

EEG REVIEW SUITE, MULTIUSE
NIHON KOHDEN AMERICA, INC.
NK-REVSUITE-MU
In Commercial Distribution

  • 00841983103650 ()
NK-REVSUITE-MU

  • Electroencephalograph

NA - 00841983103643

PHOTIC ASSEMBLY WITH STIM CONTROL
NIHON KOHDEN AMERICA, INC.
NK-LS-901AJ
In Commercial Distribution

  • 00841983103643 ()
NK-LS-901AJ

  • Electroencephalograph

Neurofax - 00841983104329

NEUROFAX ACQUISITION, SML FRM
NIHON KOHDEN AMERICA, INC.
EEG-1260A
In Commercial Distribution

  • 00841983104329 ()
EEG-1260A

  • Electroencephalograph

Vigilant Software Suite - 04052682044106

Vigilant Master Med is a component of the Vigilant Software Suite. Vigilant Master Med is part of a Dose Error Reduction System (DERS) for use with Adults, Pediatrics, and Neonates. It is intended to create, customize, and manage drug library data and device configurations to be uploaded to compatible Fresenius Kabi infusion devices which may reduce the risk of drug administration errors. It enhances safety by preventing infusion errors with the use of Dose Error Reduction System (DERS) in combination with the infusion devices.
Fresenius Kabi AG
ZK288122
In Commercial Distribution

  • 04052682044106 ()
ZK288122

  • Infusion pump medication-dosage application software
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