Primary Device ID | 07290014891005 |
NIH Device Record Key | fd2d8f04-b436-4ddd-94ea-164e2924dd2f |
Commercial Distribution Discontinuation | 2033-07-17 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SaliPen |
Version Model Number | OTC |
Company DUNS | 533732749 |
Company Name | SALIWELL LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Safe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
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 | 07290014891005 [Primary] |
QTT | Over The Counter Electrical Salivary Stimulatory System |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-11 |
Device Publish Date | 2024-07-03 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() SALIPEN 90794129 not registered Live/Pending |
Dr. Andy Wolff 2021-06-24 |
![]() SALIPEN 90794129 not registered Live/Pending |
Eng. Ben Z. Beiski 2021-06-24 |