Single Panel Pre Screen Plus Dip Card

GUDID 00851000007274

Single Panel Pre Screen Plus Dip Card Drug Combo: OXY

MERGERS MARKETING, INC.

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• Primary Device ID: 00851000007274
• NIH Device Record Key: aaf16e88-a277-4c15-b355-ed301732d81c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Single Panel Pre Screen Plus Dip Card
• Version Model Number: PS-OXY
• 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	00851000007250 [Primary]
GS1	00851000007267 [Package]; Contains: 00851000007250; Package: Inner Pack [25 Units]; In Commercial Distribution
GS1	00851000007274 [Package]; Contains: 00851000007267; Package: Case [20 Units]; In Commercial Distribution

FDA Product Code

• DJG: Enzyme Immunoassay, Opiates

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: 2017-06-20

On-Brand Devices [Single Panel Pre Screen Plus Dip Card]

• 00851000007274: Single Panel Pre Screen Plus Dip Card Drug Combo: OXY
• 10851000007097: Single Panel Pre Screen Plus Dip Card Drug Combo: ETG
• 10850557007413: Single Panel Pre Screen Plus Dip Card Drug Combo: THC
• 00850557007003: Single Panel Pre Screen Plus Dip Card Drug Combo: BUP