FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00841983103308 · Model: JE-212A · NIHON KOHDEN AMERICA, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
NA
Primary DI
00841983103308
Version / Model
JE-212A
Catalog Number
JE-212A
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
4
Public Version Date
2024-03-04
Public Version Status
Update
Public Device Record Key
3a108b5c-bd0b-496f-af71-d9f4981dbca6

Device Description

AMPLIFIER, 192 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
OLT Non-normalizing quantitative electroencephalograph software
OLV Standard polysomnograph with electroencephalograph

GMDN Terms

Code Name
46566 Neurophysiologic monitoring system

Identifiers

Type ID
Primary 00841983103308

Customer Contacts