Primary Device ID | 06971712727209 |
NIH Device Record Key | ebadafd2-41ae-4e11-8332-2bf27ec1d6ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Copper Life |
Version Model Number | TENS |
Company DUNS | 421286946 |
Company Name | Hong Qiangxing (Shen Zhen) Electronics Limited |
Device Count | 36 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06971712727209 [Unit of Use] |
GS1 | 06971712727216 [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 | 2024-08-26 |
Device Publish Date | 2024-08-16 |
16971712722973 - Numiere | 2025-02-12 |
06971712729944 - takoo | 2025-01-30 |
16971712727466 - NURSAL | 2025-01-09 HPTS0237 silver |
06971712727759 - Cloudix | 2025-01-08 |
06971727219706 - eMP10 | 2025-01-08 |
06971712729647 - TOMMIE COPPER | 2024-12-11 |
06971712727452 - TEC.BEAN | 2024-12-10 |
06971712727483 - TENKER | 2024-12-10 PURPLE |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() COPPER LIFE 90463960 not registered Live/Pending |
Behr Process Corporation 2021-01-13 |
![]() COPPER LIFE 86097016 5008439 Live/Registered |
TOMMIE COPPER IP, INC. 2013-10-21 |