Primary Device ID | 04053228010722 |
NIH Device Record Key | 8674e020-219e-40f7-96a8-7b0230a9ceef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | QIAcube |
Version Model Number | 1 |
Catalog Number | 9001292 |
Company DUNS | 317103745 |
Company Name | QIAGEN GmbH |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04053228010722 [Primary] |
JJH | Clinical Sample Concentrator |
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 | 2017-08-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() QIACUBE 79037735 3445464 Live/Registered |
QIAGEN GmbH 2006-08-28 |