| 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 |