| Primary Device ID | 20370797801017 |
| NIH Device Record Key | fbfb5727-faf7-40a2-8212-840d18dfe603 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dr. Talbot's |
| Version Model Number | 80101 |
| Company DUNS | 078855555 |
| Company Name | TALBOT'S PHARMACEUTICALS FAMILY PRODUCTS, LLC |
| 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 | 00370797801013 [Primary] |
| GS1 | 20370797801017 [Package] Contains: 00370797801013 Package: [6 Units] In Commercial Distribution |
| GS1 | 30370797801014 [Package] Package: [4 Units] In Commercial Distribution |
| JEQ | Toothbrush, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-07-23 |
| Device Publish Date | 2020-07-15 |