| Primary Device ID | E219J302648001 |
| NIH Device Record Key | 9d4c1aa5-fd1a-430a-9a39-9a6cfd39f92e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Multi-unit Implant analog |
| Version Model Number | J3026.4800 |
| Catalog Number | J3026.4800 |
| Company DUNS | 322018193 |
| Company Name | ALTATEC GmbH |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
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