Primary Device ID | 00075020087386 |
NIH Device Record Key | e07ea57e-e0c4-4aeb-8efe-c7f6bf3e7023 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips Sonicare |
Version Model Number | HX6462/06 |
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 | 00075020087386 [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 | 2020-05-07 |
Device Publish Date | 2020-04-29 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PHILIPS SONICARE 90583352 not registered Live/Pending |
Deng, Fei 2021-03-16 |