FDA UDI In Commercial Distribution 🇺🇸 United States

REMI

DI: 00860005388172 · Model: 1.x.x.x · Epitel, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REMI
Primary DI
00860005388172
Version / Model
1.x.x.x
Company Name
Epitel, Inc.
Labeler DUNS
808401157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-17
Public Version
1
Public Version Date
2023-11-27
Public Version Status
New
Public Device Record Key
13d45ce4-ddff-403c-a1c7-1c49a06c3f81

Device Description

REMI Mobile (Remote EEG Monitoring Software) - Ambulatory Use Module

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
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
OMC Reduced- Montage Standard Electroencephalograph

GMDN Terms

Code Name
38736 Electroencephalographic monitoring system

Identifiers

Type ID
Primary 00860005388172

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K230933 000