Primary Device ID | 00857031002240 |
NIH Device Record Key | 357e22b6-a155-4441-8db5-9fd7946d0c76 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GIARDIA/CRYPTOSPORIDIUM CHEK |
Version Model Number | T5031 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00857031002240 [Primary] |
MHJ | Cryptosporidium Spp. |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-23 |
00857031002240 | The GIARDIA/CRYPTOSPORIDIUM CHEK test is an enzyme immunoassay for the qualitative detection of |
00857031002127 | The GIARDIA/CRYPTOSPORIDIUM CHEK test is an enzyme immunoassay for the qualitative detection of |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GIARDIA/CRYPTOSPORIDIUM CHEK 78674453 3084001 Live/Registered |
TechLab, Inc. 2005-07-20 |