FDA UDI In Commercial Distribution 🇺🇸 United States

BodyMed

DI: 00815802014908 · Model: NPP621 · BOXOUT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
BodyMed
Primary DI
00815802014908
Version / Model
NPP621
Catalog Number
NPP621
Company Name
BOXOUT, LLC
Labeler DUNS
066689993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-05
Public Version
7
Public Version Date
2023-08-14
Public Version Status
Update
Public Device Record Key
575be910-bfc3-4b74-8b5b-7f69b75267c8

Device Description

BODYMED 2" X 2" SQUARE WHITE FOAM CARBON ELECTRODE, 4/PK

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
Yes
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
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
GXY Electrode, Cutaneous

GMDN Terms

Code Name
35995 Transcutaneous electrical stimulation electrode, single-use

Identifiers

Type ID
Primary 00815802014908
Package 10815802014905
Package 20815802014902

Customer Contacts

Phone
866-528-2152

Premarket Submissions

Submission Number Supplement Number
K092546 000
K160138 000