FDA UDI In Commercial Distribution 🇺🇸 United States

REMI

DI: 00860011072454 · Model: 20110 · Epitel, Inc.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
REMI
Primary DI
00860011072454
Version / Model
20110
Catalog Number
20110
Company Name
Epitel, Inc.
Labeler DUNS
808401157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-08-06
Public Version
1
Public Version Date
2024-08-14
Public Version Status
New
Public Device Record Key
5d8516cf-2ea9-4742-aac9-b5afa6fbbd70

Device Description

REMI Ambulatory Patient Starter Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OMC Reduced- Montage Standard Electroencephalograph
GXY Electrode, Cutaneous

GMDN Terms

Code Name
38736 Electroencephalographic monitoring system
61694 Skin cleaning wipe

Identifiers

Type ID
Primary 00860011072454

Customer Contacts

Device Sizes

Type Value Unit Text
Length 1 Inch
Width 1 Inch
Depth 0.25 Inch

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Handling Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity