| Primary Device ID | 00815696020375 |
| NIH Device Record Key | a2491f88-e34a-4e5f-9b81-8a28b27895f0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | George King FACT |
| Version Model Number | 0020-1.0 |
| Company DUNS | 066761271 |
| Company Name | GEORGE KING BIO-MEDICAL, 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 | 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 | 1-800-255-5108 |
| plasma@kingbiomed.com | |
| Phone | 1-800-255-5108 |
| plasma@kingbiomed.com | |
| Phone | 1-800-255-5108 |
| plasma@kingbiomed.com |
| Special Storage Condition, Specify | Between 0 and 0 *-70˚C or below |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00815696020375 [Primary] |
| GGN | Plasma, Coagulation Control |
| 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 | 2016-08-17 |
| 00815696020566 | George King FACT is a normal fresh frozen citrated control that is used to verify the performanc |
| 00815696020375 | George King FACT is a normal fresh frozen citrated control that is used to verify the performanc |
| 00815696020368 | George King FACT is a normal fresh frozen citrated control that is used to verify the performanc |