FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04931921103937 · Model: PE-210AK · NIHON KOHDEN CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04931921103937
Version / Model
PE-210AK
Catalog Number
PE-210AK
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
3
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
83699fae-14b4-4fbc-9806-ca8e30ea5f9b

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
GYC ELECTRODE, CORTICAL
GWQ Full-montage Standard Electroencephalograph

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary 04931921103937

Customer Contacts