Primary Device ID | 05391516746625 |
NIH Device Record Key | b6e6db83-bdd7-431a-a73b-26b60aef2d3b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MarDx |
Version Model Number | 40-8696G |
Catalog Number | 40-8696G |
Company DUNS | 623214079 |
Company Name | CLARK LABORATORIES, 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 | 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 | false |
OTC Over-The-Counter | false |
Phone | 1-800-325-3424 |
customerservice@trinityusa.com |
Device Size Text, specify | 0 |
Storage Environment Temperature | Between 2 Degrees Celsius and 8 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05391516746625 [Primary] |
LSR | Reagent, Borrelia Serological Reagent |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-11-04 |
Device Publish Date | 2019-10-25 |
05391516746649 | Borrelia burgdorferi EIA IgM |
05391516746632 | Borrelia burgdorferi EIA IgM |
05391516746618 | Borrelia burgdorferi EIA IgG + IgM |
05391516746601 | Borrelia burgdorferi EIA IgG + IgM |
05391516746625 | Borrelia burgdorferi EIA IgG |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MARDX 75802570 2490009 Live/Registered |
MarDx Diagnostics, Inc. 1999-09-17 |
MARDX 75801516 2364681 Live/Registered |
MarDx Diagnostics, Inc. 1999-09-17 |
MARDX 73649657 1512233 Dead/Cancelled |
MARDX DIAGNOSTICS, INC. 1987-03-16 |