| 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 |