FDA UDI In Commercial Distribution 🇺🇸 United States

AXUS ES-5

DI: 14897076720092 · Model: ED3930 · TENS PLUS INDUSTRIAL COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AXUS ES-5
Primary DI
14897076720092
Version / Model
ED3930
Catalog Number
ED3930
Company Name
TENS PLUS INDUSTRIAL COMPANY
Labeler DUNS
663211978
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-30
Public Version
1
Public Version Date
2021-04-07
Public Version Status
New
Public Device Record Key
6c53cf5a-700d-4d1e-a4b0-096d8d8d5da2

Device Description

The AXUS ES-5 is an electro-acupuncture device indicated for use in the practice of acupuncture by qualified professionals of acupuncture as determined by the state. The AXUS ES-5 is a battery operated prescription use only electro-acupuncture device used for applying electric stimuli to areas of preferred delivery (APD). The device uses a low-intensity, low-frequency pulse multimode generator through micro-alligator clips attached to commercially available and FDA-cleared stainless steel acupuncture needles. The device can also deliver stimulation with the included probe.

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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BWK Stimulator, Electro-Acupuncture

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Primary 14897076720092

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K200636 000