Primary Device ID | 10852359007066 |
NIH Device Record Key | bb67b1e0-bfe3-4e46-a0dc-c02478b56d60 |
Commercial Distribution Discontinuation | 2018-12-12 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | MAXCHECK |
Version Model Number | CDTC121 |
Catalog Number | CDTC121 |
Company DUNS | 066886996 |
Company Name | MAXPERT MEDICAL |
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 | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852359007069 [Primary] |
GS1 | 10852359007066 [Package] Contains: 00852359007069 Package: [25 Units] Discontinued: 2018-12-12 Not in Commercial Distribution |
GS1 | 20852359007063 [Package] Package: [4 Units] Discontinued: 2018-12-12 Not in Commercial Distribution |
LDJ | Enzyme Immunoassay, Cannabinoids |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-14 |
Device Publish Date | 2017-12-19 |
10852359007066 | 12 Panel Rapid Multi-Drug Test Cup |
20852359007049 | One Step Pregnancy (HCG) Urine Test Strip |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MAXCHECK 97073439 not registered Live/Pending |
Hefei Danneng Trading Co., Ltd 2021-10-13 |
![]() MAXCHECK 87402631 5306663 Live/Registered |
Maxpert Medical, LLC 2017-04-07 |
![]() MAXCHECK 86211304 not registered Dead/Abandoned |
Max2 Inc. 2014-03-05 |