| Primary Device ID | 20705032101049 | 
| NIH Device Record Key | 7ffbe066-b774-4b2a-b6b4-000b7b6beafa | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | BRITECROSS™ Support Catheter | 
| Version Model Number | BC14150 | 
| Catalog Number | BC14150 | 
| Company DUNS | 118274128 | 
| Company Name | Cordis US Corp. | 
| 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 | false | 
| Manufacturing Date | false | 
| Expiration Date | true | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | false | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 20705032101049 [Primary] | 
| DQY | Catheter, Percutaneous | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2025-09-09 | 
| Device Publish Date | 2025-09-01 | 
| 20705032101124 | BriteCross .035 x 190CM | 
| 20705032101117 | BriteCross .035 x 135CM | 
| 20705032101100 | BriteCross .035 x 90CM | 
| 20705032101094 | BriteCross .018 x 200CM | 
| 20705032101087 | BriteCross .018 x 150CM | 
| 20705032101070 | BriteCross .018 x 90CM | 
| 20705032101063 | BriteCross .018 x 65CM | 
| 20705032101056 | BriteCross .014 x 200CM | 
| 20705032101049 | BriteCross .014 x 150CM | 
| 20705032101032 | BriteCross .014 x 90CM | 
| 20705032101025 | BriteCross .014 x 65CM | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  BRITECROSS  98129268  not registered Live/Pending | Cordis US Corp 2023-08-11 |