Primary Device ID | 08033891329716 |
NIH Device Record Key | 139518a4-0a73-4a81-97ee-59a4a786af63 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MINI-CUBE |
Version Model Number | 10392 |
Catalog Number | 10392 |
Company DUNS | 435036669 |
Company Name | DIESSE DIAGNOSTICA SENESE SPA |
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 | true |
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 | 08033891329716 [Primary] |
GKB | Device, Automated Sedimentation Rate |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-05 |
Device Publish Date | 2022-11-25 |
08033891320010 - CHORUS ECHINOCOCCUS IgG | 2024-01-30 |
08033891320522 - VACU-TEC | 2024-01-30 |
08033891320645 - VACU-TEC CUVETTE-L | 2024-01-30 |
08033891320690 - VES-TEC CUVETTE-L | 2024-01-30 |
08033891321086 - VACU-TEC S.C. | 2024-01-30 |
08033891321093 - VACU-TEC S.C. STERILE | 2024-01-30 |
08033891322083 - CHORUS Q FEVER PHASE II IgG | 2024-01-30 |
08033891322434 - CHORUS MEASLES IgG | 2024-01-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MINI-CUBE 72388160 0925423 Dead/Expired |
AMERICAN TECHNICAL CERAMICS, DIVISION OF PHASE INDUSTRIES, INC. 1971-04-02 |
MINI-CUBE 72184054 0789056 Dead/Expired |
GENERAL ELECTRIC COMPANY 1964-01-06 |