| Primary Device ID | 00075020085948 |
| NIH Device Record Key | eb5e0948-40f3-41f1-b22f-da6cb9e5ea33 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Philips Sonicare |
| Version Model Number | HX6231/72 |
| Company DUNS | 608729869 |
| Company Name | PHILIPS ORAL HEALTHCARE, 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 | true |
| 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 | 00075020085948 [Primary] |
| 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 | 2020-04-24 |
| Device Publish Date | 2020-04-16 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PHILIPS SONICARE 90583352 not registered Live/Pending |
Deng, Fei 2021-03-16 |