Primary Device ID | 20370797801000 |
NIH Device Record Key | 2372be92-4672-44ae-8bc9-17947de62335 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dr. Talbot's |
Version Model Number | 80100 |
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 | 00370797801006 [Primary] |
GS1 | 20370797801000 [Package] Contains: 00370797801006 Package: [6 Units] In Commercial Distribution |
GS1 | 30370797801007 [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 |