| Primary Device ID | 08800023144291 |
| NIH Device Record Key | ff828441-eb59-40c4-a43c-5d470199beee |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Temporary Abutment |
| Version Model Number | ICTAHR5094ES |
| Company DUNS | 688248447 |
| Company Name | Cybermed Inc. |
| Device Count | 1 |
| 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 | true |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | false |