| Primary Device ID | 00843876000039 | 
| NIH Device Record Key | 72e7049d-72c5-4f1f-8c4d-b3bcb2bf2f5a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | CRYOcheck™ Pooled Normal Plasma | 
| Version Model Number | CCN10-10 | 
| Company DUNS | 244713368 | 
| Company Name | Precision Biologic Inc | 
| Device Count | 10 | 
| 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 | false | 
| 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 | false | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00843876000039 [Primary] | 
| GS1 | 00843876010038 [Unit of Use] | 
| GGN | Plasma, Coagulation Control | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 3 | 
| Public Version Date | 2018-07-06 | 
| Device Publish Date | 2016-09-23 | 
| 00843876000046 | CCN-40 | 
| 00843876000039 | CCN10-10 | 
| 00843876000022 | CCN-15 | 
| 00843876000015 | CCN-10 | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  CRYOCHECK  77260682  3656409 Live/Registered | PRECISION BIOLOGIC INC. 2007-08-21 |