Twelve Panel Clear Scan Drug Test Cup With Adulterants

GUDID 10851000007035

Twelve Panel Clear Scan Drug Test Cup Drug Combo: AMP | BAR | BUP | BZO | COC | MDMA | MET | MOR | MTD | OXY | PCP | THC With Adulterants

MERGERS MARKETING, INC.

Multiple drugs of abuse IVD, kit, immunochromatographic test (ICT), rapid

• Primary Device ID: 10851000007035
• NIH Device Record Key: 83b05821-bf51-4bec-9909-2249970a69f2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Twelve Panel Clear Scan Drug Test Cup With Adulterants
• Version Model Number: CSC-6125AD
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00851000007021 [Primary]
GS1	00851000007038 [Package]; Contains: 00851000007021; Package: Inner Pack [25 Units]; In Commercial Distribution
GS1	10851000007035 [Package]; Contains: 00851000007038; Package: Case [4 Units]; In Commercial Distribution

FDA Product Code

• LDJ: Enzyme Immunoassay, Cannabinoids

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-08-31

Devices Manufactured by MERGERS MARKETING, INC.

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• 00850557007140 - Five Panel Pre Screen Plus Dip Card (CLIA Waived): 2018-03-29 Five Panel PreScreen Plus Dip Card (CLIA Waived) Drug Combo: AMP | COC | MET | OPI | THC