| Primary Device ID | 05414904032992 |
| NIH Device Record Key | b2eeb61a-e14b-4d2b-91ba-d56f05e26960 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CURIX ORTHO MEDIUM |
| Version Model Number | CURIX ORTHO MEDIUM 30X40 |
| Catalog Number | 3KNS1 |
| Company DUNS | 374444883 |
| Company Name | AGFA |
| 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 | true |
| 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 |
| Phone | +1(877)777-2432 |
| salesinfo@agfa.com |
| Length | 30 Centimeter |
| Length | 30 Centimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05414904032992 [Primary] |
| IXA | Cassette, radiographic film |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-06-14 |
| Device Publish Date | 2016-09-01 |
| 05414904034026 | CURIX CAS US+OR MED 24X30 |
| 05414904034002 | CURIX CAS US+OR MED 18X24 |
| 05414904033807 | CURIX CAS US+OR MED 35X43 |
| 05414904033791 | CURIX CAS US+OR MED 35X35 |
| 05414904033784 | CURIX CAS US+OR MED 30X40 |
| 05414904033210 | CURIX CAS EU+OR MED 18X24 |
| 05414904033012 | CURIX CAS EU+OR MED 35X43 |
| 05414904033005 | CURIX CAS EU+OR MED 35X35 |
| 05414904032992 | CURIX CAS EU+OR MED 30X40 |
| 05414904032985 | CURIX CAS EU+OR MED 24X30 |
| 05414904032961 | CURIX CAS EU+OR MED 18X43 |