FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00841983104077 · Model: AE-918P-N/ZA · NIHON KOHDEN AMERICA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00841983104077
Version / Model
AE-918P-N/ZA
Catalog Number
AE-918P-N/ZA
Company Name
NIHON KOHDEN AMERICA, INC.
Labeler DUNS
021063219
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-08-29
Public Version
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
325faeb8-b9c3-4145-a493-b56253fe2ceb

Device Description

EEG POD ACCESSORY KIT 2CH NEO, AE-918

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
OMA Amplitude-integrated electroencephalograph

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary 00841983104077

Customer Contacts