Primary Device ID | 00843876000176 |
NIH Device Record Key | 38084cd3-4c93-4d6a-ad31-7eedf00519fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CRYOcheck™ Weak Lupus Positive Control |
Version Model Number | CCWLP-10 |
Company DUNS | 244713368 |
Company Name | Precision Biologic Inc |
Device Count | 25 |
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 | 00843876000176 [Primary] |
GS1 | 00843876010175 [Unit of Use] |
GGC | Control, Plasma, Abnormal |
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 |
00843876000176 | CCWLP-10 |
00843876000169 | CCWLP-05 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CRYOCHECK 77260682 3656409 Live/Registered |
PRECISION BIOLOGIC INC. 2007-08-21 |