| Primary Device ID | 20048526006216 |
| NIH Device Record Key | e258c424-0cac-4cc9-86ea-af4a8cba9ae1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nuby |
| Version Model Number | 621 |
| Company DUNS | 108926288 |
| Company Name | LUV N' CARE, 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 | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00048526006212 [Primary] |
| GS1 | 20048526006216 [Package] Contains: 00048526006212 Package: [4 Units] In Commercial Distribution |
| GS1 | 40048526006210 [Package] Package: [4 Units] In Commercial Distribution |
| KKO | Ring, Teething, Fluid-Filled |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-11-02 |
| Device Publish Date | 2020-10-23 |