| Primary Device ID | 16926338766665 |
| NIH Device Record Key | 2ee399e5-dc5c-4ce2-bd95-35cefe9f3427 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Parent’s choice |
| Version Model Number | NP-SO130F |
| Company DUNS | 530853944 |
| Company Name | Shanghai Foliage Industry 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 | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |