| Primary Device ID | 08056304451187 |
| NIH Device Record Key | fb5a2bda-cb4e-4b4c-9812-4913b12e1966 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CAAS IntraVascular |
| Version Model Number | 1.0 |
| Company DUNS | 413761941 |
| Company Name | Pie Medical Imaging 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 | 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 |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl | |
| Phone | +31308500202 |
| support@pie.nl |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08056304451187 [Primary] |
| LLZ | System, Image Processing, Radiological |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-10-07 |
| Device Publish Date | 2016-09-27 |
| 08056304451187 | 1.0 |
| 08056304454065 | 2.1 |
| 08056304453471 | 2.0 |