| Primary Device ID | 10726893111308 |
| NIH Device Record Key | 14963221-3874-4404-9b90-c38dbd9d6779 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ONE Vanish Hyperthin |
| Version Model Number | 111302 |
| Company DUNS | 364614362 |
| Company Name | GLOBAL PROTECTION CORP. |
| Device Count | 12 |
| DM Exempt | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00726893111301 [Primary] |
| GS1 | 10726893111308 [Package] Contains: 00726893111301 Package: Bundle of 3, 12 pack [3 Units] In Commercial Distribution |
| GS1 | 20726893111305 [Package] Package: 24 bundles of 3 [24 Units] In Commercial Distribution |
| GS1 | 80726893111307 [Unit of Use] |
| HIS | Condom |
| QRZ | External Condom For Anal Intercourse Or Vaginal Intercourse |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-06-23 |
| Device Publish Date | 2020-06-15 |
| 20726893111954 | Male Lubricated Latex Condoms |
| 10726893111308 | Lubricated Male Latex Condoms |
| 80726893114674 | Latex Lubricated Condoms |