| 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 |