| Primary Device ID | 00856264005318 |
| NIH Device Record Key | dc8ec023-8144-4686-9d08-2715274ff746 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Argus ll Retinal Implant Kit |
| Version Model Number | 011014-004-K |
| Catalog Number | 011014-K |
| Company DUNS | 086470742 |
| Company Name | Second Sight Medical Products, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Conditional |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00856264005318 [Primary] |
| NBF | Prosthesis,Retinal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-05-06 |
| 00856264005707 | The retinal prosthesis implant is responsible for receiving information from the external compon |
| 00856264005691 | The retinal prosthesis implant is responsible for receiving information from the external compon |
| 00856264005318 | The retinal prosthesis implant is responsible for receiving information from the external compon |
| 00856264005301 | The retinal prosthesis implant is responsible for receiving information from the external compon |