| Primary Device ID | 20787551000003 |
| NIH Device Record Key | d7f81a12-a9d8-430a-94be-2041fa7726fe |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Fog Guard Anti-Fog Solution with Sponge |
| Version Model Number | 30900 |
| Company DUNS | 868042664 |
| Company Name | XODUS MEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Safe |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00787551000009 [Primary] |
| GS1 | 20787551000003 [Package] Contains: 00787551000009 Package: [20 Units] In Commercial Distribution |
| OCT | Anti fog solution and accessories, endoscopy |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-03-28 |
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