FDA UDI In Commercial Distribution 🇺🇸 United States

Neuropack X1

DI: 04931921102169 · Model: DC-230BA · NIHON KOHDEN CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neuropack X1
Primary DI
04931921102169
Version / Model
DC-230BA
Catalog Number
DC-230BA
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
cd0ec4f3-c5d0-483c-a714-0d575fc7e3da

Device Description

Main unit for MEB-2300A

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
MR Unsafe
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 04931921102169

Customer Contacts