FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 00841983101076 · Model: PE-210AK · NIHON KOHDEN AMERICA, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
00841983101076
Version / Model
PE-210AK
Catalog Number
PE-210AK
Company Name
NIHON KOHDEN AMERICA, INC.
Labeler DUNS
021063219
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-19
Public Version
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
2356d50e-f510-4b59-991b-19c688a90d10

Device Description

Switch Box for the EEG-1200A

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
GWQ Full-montage Standard Electroencephalograph
GYC ELECTRODE, CORTICAL

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary 00841983101076

Customer Contacts