| Primary Device ID | 50048526006002 |
| NIH Device Record Key | 892abee7-dfd3-4f1d-81d3-59fd02f323dc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Nuby |
| Version Model Number | 600 |
| Company DUNS | 108926288 |
| Company Name | LUV N' CARE, LTD. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does n |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00048526006007 [Primary] |
| GS1 | 20048526006001 [Package] Contains: 00048526006007 Package: [4 Units] In Commercial Distribution |
| GS1 | 50048526006002 [Package] Contains: 20048526006001 Package: [4 Units] In Commercial Distribution |
| KKO | Ring, Teething, Fluid-Filled |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-11-02 |