| Primary Device ID | 06951740500265 |
| NIH Device Record Key | 3bee9e6a-aecf-4b97-bbe3-9a84425f26f2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | pluse oximeter |
| Version Model Number | JPD-500C |
| 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 | 06951740500197 [Primary] |
| GS1 | 06951740500265 [Package] Contains: 06951740500197 Package: [50 Units] In Commercial Distribution |
| DQA | Oximeter |
| 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 | 2016-09-24 |
| 06951740540018 | pluse oximeter（white） |
| 06951740538374 | pluse oximeter（white） |
| 06951740538367 | pluse oximeter（black） |
| 06951740500227 | JPD-500F |
| 06951740500210 | JPD-500E |
| 06951740500203 | JPD-500D |
| 06951740500265 | JPD-500C |
| 06951740500258 | JPD-500B |
| 06951740500241 | JPD-500A |
| 06951740540070 | SPA30 |
| 06951740540063 | SPA20 |
| 06951740540056 | SPA11 |
| 06951740540049 | SPA10 |