FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04931921112830 · Model: KC-001A · NIHON KOHDEN CORPORATION
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04931921112830
Version / Model
KC-001A
Catalog Number
KC-001A
Company Name
NIHON KOHDEN CORPORATION
Labeler DUNS
690568050
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-05
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
901d3c61-7982-4f06-812a-398058e1e8e5

Device Description

STAND,INPUT BOX/PHOTIC EEG-1200

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

GMDN Terms

Code Name
34909 Instrument trolley

Identifiers

Type ID
Primary 04931921112830

Customer Contacts