| Primary Device ID | E203OD031009 |
| NIH Device Record Key | 413b7d40-53cb-4cb6-a275-3926dafc6f2e |
| Commercial Distribution Discontinuation | 2019-11-05 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | PGA RESORBA |
| Version Model Number | PGA RESORBA |
| Company DUNS | 341053195 |
| Company Name | Resorba Medical GmbH |
| 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 | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| 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 |