Primary Device ID | 00857031002493 |
NIH Device Record Key | b8e18c0a-cc78-400e-9561-f4463284ad9d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | H. PYLORI QUIK CHEK |
Version Model Number | T5050 |
Company DUNS | 614218634 |
Company Name | TECHLAB, INC. |
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 |