FDA UDI Not in Commercial Distribution 🇺🇸 United States

REMI

DI: 00860011072461 · Model: ab3.x.x · Epitel, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REMI
Primary DI
00860011072461
Version / Model
ab3.x.x
Catalog Number
20039
Company Name
Epitel, Inc.
Labeler DUNS
808401157
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-06
Public Version
2
Public Version Date
2025-02-11
Public Version Status
Update
Public Device Record Key
0b3e2300-c624-4afd-a54a-0cc3466833d1
Distribution End Date
2024-12-31

Device Description

REMI Server

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
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 00860011072461

Customer Contacts