FDA UDI In Commercial Distribution 🇺🇸 United States

MODO

DI: 00841983103704 · Model: A/NIH8000 · NIHON KOHDEN AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MODO
Primary DI
00841983103704
Version / Model
A/NIH8000
Catalog Number
A/NIH8000
Company Name
NIHON KOHDEN AMERICA, INC.
Labeler DUNS
021063219
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2023-10-09
Public Version Status
Update
Public Device Record Key
183e2099-b82a-4a13-a64c-e92940f36106

Device Description

CART FOR EEG-9200 / 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
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
OLT Non-normalizing quantitative electroencephalograph software

GMDN Terms

Code Name
34909 Instrument trolley

Identifiers

Type ID
Primary 00841983103704

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080546 000