| Primary Device ID | 04049471100020 |
| NIH Device Record Key | 0189bdf9-f20e-4b52-accc-b6150d68bf7c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FORUM Viewer App |
| Version Model Number | FORUM Viewer App |
| Company DUNS | 314594680 |
| Company Name | Carl Zeiss Meditec AG |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| 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 | 04049471100020 [Primary] |
| NFG | Device, Communications, Images, Ophthalmic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-04-23 |
| Device Publish Date | 2018-03-22 |
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