FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00841983103551 · Model: A/NIH9000 · NIHON KOHDEN AMERICA, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00841983103551
Version / Model
A/NIH9000
Catalog Number
A/NIH9000
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
33762593-546c-4218-a478-f7e265778909

Device Description

CART FOR MEB-9400, MEB-2300, MEE-1000 and MEE-2000 desktop systems

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
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
IKN Electromyograph, diagnostic
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE

GMDN Terms

Code Name
34909 Instrument trolley

Identifiers

Type ID
Primary 00841983103551

Customer Contacts