| Primary Device ID | 06951740501644 |
| NIH Device Record Key | d14ad772-9068-4627-8fa4-810a7e52fb02 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Morpilot |
| Version Model Number | JPD-FR401 |
| Company DUNS | 529217911 |
| Company Name | Shenzhen Jumper Medical Equipment Co.,Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06951740501644 [Primary] |
| FLL | Thermometer, Electronic, Clinical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-05-19 |
| 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 |
|---|---|
![]() MORPILOT 98266766 not registered Live/Pending |
Keenstone Corp. 2023-11-13 |
![]() MORPILOT 86849774 5098791 Live/Registered |
Keenstone Corp. 2015-12-15 |