| Primary Device ID | 37613327055291 |
| NIH Device Record Key | 291cfb0a-3365-4529-96da-b952beb8624c |
| Commercial Distribution Discontinuation | 2016-12-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Fluid Safe |
| Version Model Number | 0502100000 |
| Catalog Number | 0502-100-000 |
| Company DUNS | 187502109 |
| Company Name | STRYKER CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | 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(866)624-4422 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327055290 [Primary] |
| GS1 | 37613327055291 [Package] Contains: 07613327055290 Package: pack [36 Units] Discontinued: 2016-12-02 Not in Commercial Distribution |
| KDQ | BOTTLE, COLLECTION, VACUUM |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-23 |
| 07613327058123 | Fluid Management System, Weighing System |
| 07613327058116 | Fluid Management System, Pump Unit |
| 37613327055840 | Fluid Management System, Integrated Tube Set, Do not use if package is damaged, Keep dry, Keep a |
| 37613327055291 | 3000 CC, Suction Canister |