FDA UDI In Commercial Distribution 🇺🇸 United States

Nihon Kohden, EEG-1200A Series Neurofax

DI: 04931921007693 · Model: KC-001A-01 · NIHON KOHDEN CORPORATION
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Nihon Kohden, EEG-1200A Series Neurofax
Primary DI
04931921007693
Version / Model
KC-001A-01
Catalog Number
KC-001A-01
Company Name
NIHON KOHDEN CORPORATION
Labeler DUNS
690568050
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-07-24
Public Version
1
Public Version Date
2019-08-01
Public Version Status
New
Public Device Record Key
63911d2e-57e5-4360-9b3e-568c6148a404

Device Description

Cart (Stand), used with Electrode junction box or Flash lamp assembly

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
OLT Non-normalizing quantitative electroencephalograph software
GWQ Full-montage Standard Electroencephalograph
OLV Standard polysomnograph with electroencephalograph
GWC ANTISERA, ALL TYPES, STREPTOCOCCUS PNEUMONIAE

GMDN Terms

Code Name
34909 Instrument trolley

Identifiers

Type ID
Primary 04931921007693

Customer Contacts