FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04931921101292 · Model: AE-918P · NIHON KOHDEN CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04931921101292
Version / Model
AE-918P
Catalog Number
AE-918P
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
5
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
bfa9df9c-0a0f-43e7-9533-a5d80e6811ab

Device Description

Neuro unit, 8 channel

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
OMA Amplitude-integrated electroencephalograph

GMDN Terms

Code Name
33586 General-purpose multi-parameter bedside monitor

Identifiers

Type ID
Primary 04931921101292

Customer Contacts