Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived)

GUDID 10851000007110

Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP | BAR | BZO | COC | MDMA | MET | MOP | MTD | OXY | PCP| TCA | THC + AD

MERGERS MARKETING, INC.

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Primary Device ID10851000007110
NIH Device Record Key07a0835c-2950-4aa9-bb73-35c55032a822
Commercial Distribution StatusIn Commercial Distribution
Brand NameTwelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived)
Version Model NumberPSC-DOA-7125AD
Company DUNS065602744
Company NameMERGERS MARKETING, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100851000007106 [Primary]
GS100851000007113 [Package]
Contains: 00851000007106
Package: Inner Pack [25 Units]
In Commercial Distribution
GS110851000007110 [Package]
Contains: 00851000007113
Package: Case [4 Units]
In Commercial Distribution

FDA Product Code

LFGRadioimmunoassay, Tricyclic Antidepressant Drugs

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-26

On-Brand Devices [Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived)]

10851000007110Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP | BAR | BZO | COC
00850557007706Twelve Panel PreScreen Plus Cup With Adulterants (CLIA Waived) Drug Combo: AMP | BAR | BUP | BZO

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