FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04931921104163 · Model: QI-120A · NIHON KOHDEN CORPORATION
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04931921104163
Version / Model
QI-120A
Catalog Number
QI-120A
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
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
8b5ffd91-ab55-4746-aee7-036dd8fb6806

Device Description

Camera Capture Unit

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
Yes
Has Lot/Batch Number
No
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
GWQ Full-montage Standard Electroencephalograph
OLT Non-normalizing quantitative electroencephalograph software
OLV Standard polysomnograph with electroencephalograph

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary 04931921104163

Customer Contacts