| Primary Device ID | 38033178113107 |
| NIH Device Record Key | 01304f2e-19c6-4b28-a02b-6f7c54ec63c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | B-CAPTA |
| Version Model Number | 3/8" VENOUS CUVETTE |
| Company DUNS | 442126587 |
| Company Name | SORIN GROUP ITALIA SRL |
| 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 | 08033178113106 [Primary] |
| GS1 | 38033178113107 [Package] Contains: 08033178113106 Package: BOX [10 Units] In Commercial Distribution |
| DRY | MONITOR, BLOOD-GAS, ON-LINE, CARDIOPULMONARY BYPASS |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-05-13 |
| Device Publish Date | 2021-05-05 |
| 38033178113527 | 3/8" ARTERIAL CUVETTE |
| 38033178113510 | 1/4" ARTERIAL CUVETTE |
| 38033178113114 | 1/2" VENOUS CUVETTE |
| 38033178113107 | 3/8" VENOUS CUVETTE |
| 38033178113091 | 1/4" VENOUS CUVETTE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() B-CAPTA 79240105 5724415 Live/Registered |
SORIN GROUP ITALIA S.R.L. 2018-06-28 |