Primary Device ID | 10451906191090 |
NIH Device Record Key | 1b37e620-8411-45c4-b3e2-497fc7e8dffa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | OasisSpace |
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 | 10451906191090 [Primary] |
GS1 | 72190619109007 [Unit of Use] |
GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2019-07-24 |
16971712726094 - Nuemedics | 2025-05-29 Elite |
16971712724748 - Techcare | 2025-05-22 Touch X |
16971712724786 - Unimed | 2025-05-22 Pro X |
16971712726087 - Nuemedics | 2025-05-22 BLACK |
16971712726100 - Nuemedics | 2025-05-22 BLACK COMBO SET |
16971712720276 - Techcare | 2025-05-21 BLACK |
16971712724724 - Techcare | 2025-05-21 BLACK COMBO SET |
16971712725509 - Techcare | 2025-05-21 RED |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() OASISSPACE 98440408 not registered Live/Pending |
MAXLEAD INNOVATIONS CO., LTD 2024-03-08 |
![]() OASISSPACE 87592942 5506544 Live/Registered |
Gold Kernal LLC 2017-09-01 |