| Primary Device ID | 00075020084088 |
| NIH Device Record Key | 61b21faf-279c-45f9-be98-53ba2bf0baf0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Philips Sonicare |
| Version Model Number | HX8492/42 |
| 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 | 00075020084088 [Primary] |
| EFS | UNIT, ORAL IRRIGATION |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-06-11 |
| Device Publish Date | 2020-06-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PHILIPS SONICARE 90583352 not registered Live/Pending |
Deng, Fei 2021-03-16 |