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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 - 00841983102585

Input box converter, EEG-1200A
NIHON KOHDEN AMERICA, INC.
QI-122A
In Commercial Distribution

  • 00841983102585 ()
QI-122A

  • Electroencephalograph

NA - 00841983102486

Flat Pack Mini Expansion, Channel 193-256
NIHON KOHDEN AMERICA, INC.
JE-228AK
In Commercial Distribution

  • 00841983102486 ()
JE-228AK

  • Electroencephalograph

Neurofax - 00841983102417

Neurofax Electroencephalograph
NIHON KOHDEN AMERICA, INC.
EEG-1200A
In Commercial Distribution

  • 00841983102417 ()
EEG-1200A

  • Electroencephalograph

NA - 00841983101304

EEG trend program
NIHON KOHDEN AMERICA, INC.
QP-160AK
In Commercial Distribution

  • 00841983101304 ()
QP-160AK

  • Electroencephalograph

NA - 00841983101106

Analog output unit
NIHON KOHDEN AMERICA, INC.
QD-120A
In Commercial Distribution

  • 00841983101106 ()
QD-120A

  • Electroencephalograph

NA - 00841983100963

Photic stimulator control unit
NIHON KOHDEN AMERICA, INC.
LS-120AJ
In Commercial Distribution

  • 00841983100963 ()
LS-120AJ

  • Electroencephalograph

NA - 00841983100895

CART, COMPACT TYPE, EEG-1200A
NIHON KOHDEN AMERICA, INC.
KE-122A
In Commercial Distribution

  • 00841983100895 ()
KE-122A

  • Instrument trolley

NA - 00841983100284

ADAPTER DUAL MOUNT, PHOTIC / INPUT
NIHON KOHDEN AMERICA, INC.
DI-120A
In Commercial Distribution

  • 00841983100284 ()
DI-120A

  • Instrument trolley

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

nuance audio - 08059820279921

No Description
LUXOTTICA GROUP SPA
AW5004656
In Commercial Distribution

  • 08059820279921 ()


  • Air-conduction hearing aid, spectacle
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