Primary Device ID | 00810026143762 |
NIH Device Record Key | 1f6ef3d1-e78c-494d-a64a-126ea39805fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 4Patriots |
Version Model Number | 1 |
Company DUNS | 080151965 |
Company Name | 4PATRIOTS, 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 | true |
Lot Batch | true |
Serial Number | false |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810026143762 [Primary] |
LLR | Sponge, Contraceptive |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-05-18 |
Device Publish Date | 2020-05-08 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() 4PATRIOTS 88199773 5918223 Live/Registered |
Avalon Group, LLC 2018-11-19 |