FDA UDI In Commercial Distribution 🇺🇸 United States

1BYONE

DI: 00858069007016 · Model: 725EU-0002 · 1BYONEPRODUCTS INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
1BYONE
Primary DI
00858069007016
Version / Model
725EU-0002
Company Name
1BYONEPRODUCTS INC.
Labeler DUNS
845019202
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-24
Public Version
5
Public Version Date
2022-03-14
Public Version Status
Update
Public Device Record Key
8ad3bc40-ac4d-4dac-b406-67e31dd15a6c

Device Description

Electronic Pulse Stimulator Replacement Pads 4x4cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
NGX Stimulator, Muscle, Powered, For Muscle Conditioning

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Package 10858069007020
Package 00858069007023
Primary 00858069007016

Premarket Submissions

Submission Number Supplement Number
K153520 000