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 |