| Primary Device ID | 06951740517959 |
| NIH Device Record Key | c296e470-ff26-4e81-8f5b-1b2b04cb60aa |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PUREMED |
| Version Model Number | JPD-HA200C |
| Company DUNS | 529217911 |
| Company Name | Shenzhen Jumper Medical Equipment Co.,Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 06951740517959 [Primary] |
| DXN | System, Measurement, Blood-Pressure, Non-Invasive |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-12 |
| Device Publish Date | 2023-12-04 |
| 06951740540360 - NOVA | 2025-08-15 |
| 06951740518147 - JUMPER | 2025-05-19 |
| 06951740520188 - JUMPER | 2025-05-19 |
| 06951740500562 - JUMPER | 2025-04-10 |
| 06951740500579 - JUMPER | 2025-04-10 |
| 06951740517935 - JUMPER | 2025-04-10 |
| 06951740517942 - JUMPER | 2025-04-10 |
| 06951740520171 - JUMPER | 2025-02-17 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PUREMED 98721123 not registered Live/Pending |
SPIELBERG, MAX 2024-08-28 |
![]() PUREMED 88725881 not registered Live/Pending |
SHENZHEN EJ TECHNOLOGY CO., LTD 2019-12-13 |
![]() PUREMED 77201723 3772049 Live/Registered |
Georgia Gulf Corporation 2007-06-08 |