| Primary Device ID | 00726893112575 |
| NIH Device Record Key | 93528f77-3d8e-4a72-a6de-ddd87eb00fb1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Trojan Ultra Ribbed Condom |
| Version Model Number | 00726893112575 |
| Company DUNS | 001211952 |
| Company Name | CHURCH & DWIGHT CO., INC. |
| Device Count | 3 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | +1(800)833-9532 |
| Consumer.Relations@churchdwight.com | |
| Phone | +1(800)833-9532 |
| Consumer.Relations@churchdwight.com | |
| Phone | +1(800)833-9532 |
| Consumer.Relations@churchdwight.com | |
| Phone | +1(800)833-9532 |
| Consumer.Relations@churchdwight.com | |
| Phone | +1(800)833-9532 |
| Consumer.Relations@churchdwight.com | |
| Phone | +1(800)833-9532 |
| Consumer.Relations@churchdwight.com | |
| Phone | +1(800)833-9532 |
| Consumer.Relations@churchdwight.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00726893112575 [Primary] |
| GS1 | 80022600937520 [Unit of Use] |
| HIS | CONDOM |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-01-16 |
| Device Publish Date | 2020-01-08 |
| 00726893112582 | For Contraception Plus STI Protection |
| 00726893112575 | For Contraception Plus STI Protection |
| 80022600945525 | For Contraception Plus STI Protection |