| Primary Device ID | 06971922130080 |
| NIH Device Record Key | b5678845-bf3e-4820-abf1-00e86a326225 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pupilometer |
| Version Model Number | HX-400 |
| Company DUNS | 547954649 |
| Company Name | Chongqing Yeasn Science & Technology 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 | false |
| Serial Number | false |
| Manufacturing Date | false |
| 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 | 06971922130080 [Primary] |
| HLH | Pupillometer, Manual |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-10-30 |
| Device Publish Date | 2020-10-22 |
| 06971922135030 - YEASN | 2022-08-04 For eye examination and aid in the diagnosis. Contraindications: none. Target groups of patients: adults, children. Intended use |
| 06971922131070 - YEASN | 2022-04-29 |
| 06971922131674 - YEASN | 2022-04-29 |
| 06971922131728 - YEASN | 2022-04-29 |
| 06971922131926 - YEASN | 2022-04-29 |
| 06971922132725 - YEASN | 2022-04-29 |
| 06971922132732 - YEASN | 2022-04-29 |
| 06971922133029 - YEASN | 2022-04-29 |