FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04931921112809 · Model: JJ-230B · NIHON KOHDEN CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04931921112809
Version / Model
JJ-230B
Catalog Number
JJ-230B
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
24d559b5-6a7d-4bd2-a960-ef4b9731b0db

Device Description

Multi Interface Box

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

GMDN Terms

Code Name
11614 Evoked-potential graphic recording system

Identifiers

Type ID
Primary 04931921112809

Customer Contacts