FDA UDI In Commercial Distribution 🇺🇸 United States

OmniPro System

DI: B62571883000 · Model: OmniPro EEG System · Mays & Asscoiates
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
OmniPro System
Primary DI
B62571883000
Version / Model
OmniPro EEG System
Catalog Number
718-8300
Company Name
Mays & Asscoiates
Labeler DUNS
101772069
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-09
Public Version
2
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
6f5acac4-4075-4a9e-9734-5ece04185f86

Device Description

OmniPro EEG System used in EEG physiological data collection

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary B62571883000

Customer Contacts

Phone
6159732027

Premarket Submissions

Submission Number Supplement Number
K050143 000