FDA UDI In Commercial Distribution 🇺🇸 United States

RESERV

DI: 00815991021466 · Model: NPP822U10 · BOXOUT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
RESERV
Primary DI
00815991021466
Version / Model
NPP822U10
Catalog Number
CM5050FC
Company Name
BOXOUT, LLC
Labeler DUNS
066689993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-19
Public Version
7
Public Version Date
2023-07-07
Public Version Status
Update
Public Device Record Key
21ad57b0-ca21-4998-bba8-a520c177875a

Device Description

RESERV 2X2 SELF-ADHERING ELECTRODES

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXY Electrode, Cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 00815991021466
Package 10815991021463
Package 20815991021460

Customer Contacts

Phone
866-528-2152