| Primary Device ID | 37613327055208 |
| NIH Device Record Key | f852e53a-0b2d-4d4f-b650-c5b6178a1cda |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CrossFlow |
| Version Model Number | 0450000100 |
| Catalog Number | 0450-000-100 |
| Company DUNS | 187502109 |
| Company Name | STRYKER 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 | 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 |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327055207 [Primary] |
| GS1 | 37613327055208 [Package] Contains: 07613327055207 Package: pack [10 Units] In Commercial Distribution |
| HRX | ARTHROSCOPE |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2016-09-23 |
| 37613327261036 | Patient-Use Tubing, Do not use if package is damaged |
| 37613327261029 | Day-Use Inflow Cassette Tubing, Do not use if package is damaged |
| 07613327058079 | Stryker Console Customizer |
| 07613327058062 | Footswitch |
| 07613327058048 | Integrated Arthroscopy Pump |
| 37613327055222 | Integrated Cassette Tubing, Do not use if package is damaged |
| 37613327055215 | Outflow Cassette Tubing, Do not use if package is damaged |
| 37613327055208 | Inflow Cassette Tubing, Do not use if package is damaged |