FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 04931921130384 · Model: DH-120A · NIHON KOHDEN CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
04931921130384
Version / Model
DH-120A
Company Name
NIHON KOHDEN CORPORATION
Labeler DUNS
690568050
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-24
Public Version
4
Public Version Date
2023-10-09
Public Version Status
Update
Public Device Record Key
93845348-1f7a-47fa-9a31-829bc22f5f8a

Device Description

Holder

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
Yes
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
OLV Standard polysomnograph with electroencephalograph

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary 04931921130384

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171124 000