Primary Device ID | 00850557007607 |
NIH Device Record Key | 5fc94084-dfdb-46cd-b593-ab68e4d83b29 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived) |
Version Model Number | PSC-DOA-4104AD |
Company DUNS | 065602744 |
Company Name | MERGERS MARKETING, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850557007607 [Primary] |
GS1 | 00850557007614 [Package] Package: Inner Pack [25 Units] In Commercial Distribution |
GS1 | 10850557007611 [Package] Contains: 00850557007614 Package: Case [4 Units] In Commercial Distribution |
LDJ | Enzyme Immunoassay, Cannabinoids |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-07-25 |
00850557007645 | Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: BAR | BUP | BZO | COC | |
00850557007607 | Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP | BAR | BZO | COC | |
00850557007560 | Ten Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP | BAR | BZO | COC | |