Primary Device ID | 30014613201229 |
NIH Device Record Key | 27128955-c6d4-4d39-98f6-fcd26cf478a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | QuickVue+ |
Version Model Number | 20122 |
Catalog Number | 20122 |
Company DUNS | 079509836 |
Company Name | QUIDEL CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
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 |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com | |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com | |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com | |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com | |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com | |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com | |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com | |
Phone | +1(858)552-1100 |
technicalsupport@quidel.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 30014613201229 [Primary] |
GTZ | ANTISERA, ALL GROUPS, STREPTOCOCCUS SPP. |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-12-11 |
Device Publish Date | 2018-11-10 |
30014613201229 | QkVue+ Strep A, 25T |
30014613201212 | QuickVue+ Mononucleosis 20T |
30014613001799 | QkVue+ hCG S/U, 90T |
30014613001782 | QkVue+ hCG S/U, 30T |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
QUICKVUE+ 76415283 2749808 Live/Registered |
QUIDEL CORPORATION 2002-06-05 |