| Primary Device ID | M424RBYPODJ450 |
| NIH Device Record Key | 539b21c5-9fd7-4287-a539-0330b8e1efb9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | POD |
| Version Model Number | RBYPODJ45 |
| Company DUNS | 191077671 |
| Company Name | PENUMBRA, 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 | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00814548016726 [Secondary] |
| HIBCC | M424RBYPODJ450 [Primary] |
| HCG | DEVICE, NEUROVASCULAR EMBOLIZATION |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2022-08-05 |
| Device Publish Date | 2016-08-01 |
| 00814548019673 | POD, 14x60 |
| 00814548019666 | POD, 12x60 |
| 00814548019659 | POD, 10x60 |
| 00814548019642 | POD, 9x60 |
| 00814548019635 | POD, 8x60 |
| 00814548019628 | POD, 7x60 |
| 00814548019611 | POD, 6x50 |
| 00814548019604 | POD, 5x30 |
| 00814548019598 | POD, 4x30 |
| 00814548019581 | POD, 3x20 |
| 00814548017679 | RBYPODJ60 |
| 00814548017662 | RBYPODJ45 |
| 00814548017655 | RBYPODJ30 |
| 00814548017648 | RBYPODJ15 |
| 00814548017631 | RBYPODJ5 |
| 00815948020351 | POD Neuro, 6x50 |
| 00815948020344 | POD Neuro, 5x30 |
| 00815948020337 | POD Neuro, 4x30 |
| 00815948020320 | POD Neuro, 3x20 |
| M424RBYPODJ450 | RBYPODJ45 |