| Primary Device ID | B24522000GIFA1 | 
| NIH Device Record Key | 6f1ce15f-6313-48f6-83c6-a84019e41434 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | SSCOR/board | 
| Version Model Number | 22000-GIFA | 
| Company DUNS | 131254971 | 
| Company Name | SSCOR, INC. | 
| 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 | false | 
| Lot Batch | false | 
| Serial Number | true | 
| Manufacturing Date | false | 
| Expiration Date | false | 
| Donation Id Number | false | 
| Contains Natural Rubber Latex | false | 
| Labeled No Natural Rubber Latex | true | 
| RX Perscription | false | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| HIBCC | B24522000GIFA1 [Primary] | 
| GCX | Apparatus, Suction, Operating-Room, Wall Vacuum Powered | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-08-23 | 
| Device Publish Date | 2016-09-16 | 
| B245250001 | Onboard Suction Device | 
| B24523001WCKK1 | Onboard Suction Device | 
| B24523001WCK15 | Onboard Suction Device | 
| B24523001WC1 | Onboard Suction Device | 
| B24523001PLC1 | Onboard Suction Device | 
| B24523001B1 | Onboard Suction Device | 
| B245230011 | Onboard Suction Device | 
| B245225001 | Onboard Suction Device | 
| B24522020LDR12 | Onboard Suction Device | 
| B24522000RRC15 | Onboard Suction Device | 
| B24522000PLC1 | Onboard Suction Device | 
| B24522000GIFA1 | Onboard Suction Device | 
| B24522000BRAUN1 | Onboard Suction Device | 
| B245220001 | Onboard Suction Device |