Primary Device ID | 04719871185001 |
NIH Device Record Key | ee60ec28-88df-43a9-af7d-3069c6836578 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Liberty |
Version Model Number | TENS 3 |
Company DUNS | 657383535 |
Company Name | EVERYWAY MEDICAL INSTRUMENTS CO., LTD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04719871185001 [Primary] |
GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-22 |
Device Publish Date | 2022-04-14 |
04719871185001 | Transcutaneous Electrical Nerve Stimulator (T.E.N.S.) |
04719871185018 | Electrical Muscel Stimulator (EMS) |