| Primary Device ID | 00884838054257 |
| NIH Device Record Key | b5d64dea-3f4d-4499-b274-c0c4d57f524b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Allura Xper FD |
| Version Model Number | Allura Xper FD10/10 OR Table |
| Catalog Number | 722034 |
| Company DUNS | 413819707 |
| Company Name | Philips Medical Systems Nederland B.V. |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| 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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