| Primary Device ID | 05414904033791 | 
| NIH Device Record Key | ad80b34a-af8b-4e2c-b3dc-520b34f137be | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | CURIX ORTHO MEDIUM | 
| Version Model Number | CURIX ORTHO MEDIUM 35X35 | 
| Catalog Number | 3KTQN | 
| 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 | 35 Centimeter | 
| Length | 35 Centimeter | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 05414904033791 [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 |