| Primary Device ID | 10607915117020 | 
| NIH Device Record Key | a91cb0c7-95f9-4fd7-b52f-dd28ce8f472a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Suction Irrigation System | 
| Version Model Number | C6005 | 
| Company DUNS | 187129135 | 
| Company Name | APPLIED MEDICAL RESOURCES 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 | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Phone | 1.949.713.8300 | 
| contact@appliedmedical.com | |
| Phone | 1.949.713.8300 | 
| contact@appliedmedical.com | |
| Phone | 1.949.713.8300 | 
| contact@appliedmedical.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00607915117023 [Primary] | 
| GS1 | 10607915117020 [Package] Contains: 00607915117023 Package: [12 Units] In Commercial Distribution  | 
| FHF | System, Evacuator, Fluid | 
| 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 | 2016-08-18 | 
| 10607915117020 | Valve only with 12'' tubing | 
| 10607915117006 | Valve only with dual bag tubing. | 
| 10607915116986 | Probe and Valve with dual bag tubing. | 
| 00607915146504 | Valve with dual bag tubing. | 
| 00607915146498 | Probe and Valve with dual bag tubing. |