FDA UDI In Commercial Distribution 🇺🇸 United States

QuickVue TLI H. pylori Stool Antigen Test

DI: 00857031002622 · Model: 20343 · TECHLAB, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
QuickVue TLI H. pylori Stool Antigen Test
Primary DI
00857031002622
Version / Model
20343
Company Name
TECHLAB, INC.
Labeler DUNS
614218634
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-26
Public Version
1
Public Version Date
2019-10-04
Public Version Status
New
Public Device Record Key
b8f30c7b-5e4d-40e8-bd3e-8892076cdc8e

Device Description

The QuickVue TLI H. pylori Stool Antigen Test is a rapid membrane enzyme immunoassay for the qualitative detection of Helicobacter pylori specific antigen in a single use cassette. It is intended for use with human fecal specimens to aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment. The test can be used with unpreserved fecal specimens and fecal specimens preserved in transport media from patients suspected of H. pylori infection. Testing of patients to demonstrate loss of H. pylori antigen following treatment should be performed no sooner than 4 weeks after completion of the treatment regimen. Test results should be taken into consideration by the physician in conjunction with the patient history and symptoms.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYR Helicobacter Pylori

GMDN Terms

Code Name
50994 Helicobacter pylori antigen IVD, kit, enzyme immunoassay (EIA)

Identifiers

Type ID
Primary 00857031002622

Premarket Submissions

Submission Number Supplement Number
K181379 000