| Primary Device ID | 50699753270157 |
| NIH Device Record Key | 89665398-5f8f-4d94-aea8-2142a945e5ff |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CDI™ H/S Cuvette 3/8 x 3/8 |
| Version Model Number | 6913 |
| Company DUNS | 177655466 |
| Company Name | Terumo Cardiovascular Systems Corporation |
| 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 | false |
| 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 | 00699753270152 [Primary] |
| GS1 | 30699753270153 [Package] Contains: 00699753270152 Package: 20 Piece Case [20 Units] In Commercial Distribution |
| GS1 | 50699753270157 [Package] Contains: 30699753270153 Package: 6 Piece Case [6 Units] In Commercial Distribution |
| DRY | Monitor, Blood-Gas, On-Line, Cardiopulmonary Bypass |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-10-06 |