| Primary Device ID | 00851714007072 |
| NIH Device Record Key | 2db59dc1-58a9-4b24-9196-06e5e1e3dfbd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Norlake |
| Version Model Number | NSBR522WWG/0 |
| Company DUNS | 006169189 |
| Company Name | NOR-LAKE, INCORPORATED |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851714007072 [Primary] |
| KSE | Refrigerator, Freezer, Blood Storage |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-06-26 |
| Device Publish Date | 2016-10-10 |
| 00851714007089 | NSBR803WWG/0 |
| 00851714007072 | NSBR522WWG/0 |
| 00851714007065 | NSBR331WWG/0 |
| 00851714007058 | NSBR241WWG/0 |
| 00851714007041 | NSBR041WMG/0 |
| 00851714007034 | NSBF482WWW/0 |
| 00851714007027 | NSBF221WWW/0 |
| 00851714007010 | NSBF211WWW/0 |
| 00851714007003 | NSBF041WMW/0 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() NORLAKE 76198704 2653484 Live/Registered |
Nor-Lake, Incorporated 2001-01-23 |