| Primary Device ID | 40048526069376 |
| NIH Device Record Key | 7946f2a9-838c-4989-b608-1f80c356c43d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nuby |
| Version Model Number | 6937 |
| 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 | 00048526069378 [Primary] |
| GS1 | 40048526069376 [Package] Contains: 00048526069378 Package: [4 Units] In Commercial Distribution |
| GS1 | 50048526069373 [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 | 2021-08-23 |
| Device Publish Date | 2021-08-13 |