ISIS

Primary DI
04250307601424
Brand
ISIS
Company
inomed Medizintechnik GmbH
Model
504006
Device description
ISIS Xpress
Published
2022-09-16
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
ETNStimulator, Nerve
GWEStimulator, Photic, Evoked Response
GWFStimulator, Electrical, Evoked Response
GWJStimulator, Auditory, Evoked Response
GWQFull-Montage Standard Electroencephalograph
IKNElectromyograph, Diagnostic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
ETNStimulator, NerveEar, Nose, Throat2
GWEStimulator, Photic, Evoked ResponseNeurology2
GWFStimulator, Electrical, Evoked ResponseNeurology2
GWJStimulator, Auditory, Evoked ResponseNeurology2
GWQFull-Montage Standard ElectroencephalographNeurology2
IKNElectromyograph, DiagnosticPhysical Medicine2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
04250307601424PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
04250307601424042503076014244250307601424

GMDN Terms#

Term, Definition table
TermDefinition
Nerve-function monitorA mains electricity (AC-powered) bedside device designed to continuously assess the adequacy of the nerve function of a non-ambulatory patient who requires monitoring (e.g., as a result of trauma, anaesthesia, intervention, evaluation). It typically monitors evoked potential (EP), electromyography (EMG), electroencephalography (EEG) and/or neuromuscular block response. It typically consists of electrodes applied to the patient intended to acquire the neural electrical signal, and a computerized unit to process and display the information; stimulation systems for nerve block and evoked potential evaluation are separate requirements.

Regulatory Flags#

DUNS number
340782259
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
04250307604388N/A5346442026-10-01
04250307604425N/A5346722026-10-01
04250307604449N/A5346742026-10-01
04250307613526N/A5346472026-10-01
04250307613533N/A5346482026-10-01
04250307613540N/A5346762026-10-01
04250307607280ISIS5040042022-09-16
04250307607297ISIS5040052022-09-16
04250307607440ISIS5041802022-09-05
04250307607563ISIS5042852022-09-05
04250307608997ISIS5042612022-09-05
04250307609000ISIS5042712022-09-05
04250307609017ISIS5042812022-09-05
04250307609949N/A5140-522-6062019-12-17
04250307610075N/A5140-532-6312019-12-17
04250307610105N/A5140-532-6382019-12-17
04250307610167N/A5140-533-6362019-12-17
04250307610181N/A5140-530-6552019-12-17
04250307610198N/A5140-530-6562019-12-17
04250307612871Adapter cable touchproof for ALM Tube5308622026-05-29

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04250307604449N/Ainomed Medizintechnik GmbHGWF2026-10-01
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