VeriCheck Drug Test Cup VC-C05-001-35

GUDID 00870266000416

AMP1000 COC300 OPI2000 PCP25 THC50

Verify Diagnostics Inc

Multiple drugs of abuse IVD, kit, rapid ICT, clinical

• Primary Device ID: 00870266000416
• NIH Device Record Key: 524d5235-2009-427d-a579-d090dbb0db75
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VeriCheck Drug Test Cup
• Version Model Number: 1.0
• Catalog Number: VC-C05-001-35
• Company DUNS: 202753687
• Company Name: Verify Diagnostics Inc
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com
• Phone: +1 705-812-4957
• Email: support@verifydiagnostics.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit
• Storage Environment Temperature: Between 35.6 Degrees Fahrenheit and 86 Degrees Fahrenheit

Device Identifiers

Device Issuing Agency	Device ID
GS1	00870266000416 [Primary]

FDA Product Code

• NGG: Test, Methamphetamine, Over The Counter

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-25
• Device Publish Date: 2024-03-15

On-Brand Devices [VeriCheck Drug Test Cup]

• 00870266000720: CLIA Waived Drug Test Cup - 12 Panels
• 00870266001000: AMP500 BAR300 BUP10 BZO300 COC150 EDDP300 MDMA500 MET500 OPI300 OXY100 PCP25 THC50
• 00870266000737: AMP500 BAR300 BUP10 BZO300 COC150 MET500 MDMA500 OPI300 MTD300 OXY100 PCP25 THC50 CR PH SG
• 00870266000706: VeriCheck 12-panel Cup AMP500 BAR300 BZO300 COC150 MDMA500 MET500 MTD300 OPI2000 OXY100 PCP25 PP
• 00870266000584: AMP1000 BAR300 BZO300 COC300 MET1000 MTD300 OPI2000 OXY100 PCP25 THC50
• 00870266000515: AMP500 COC150 MET500 MDMA500 OPI2000 OXY100 PCP25 THC50
• 00870266000508: AMP500 COC150 MET500 MDMA500 OPI2000 PCP25 THC50 CR SG PH NI OX GL
• 00870266000492: AMP500 COC150 MET500 MDMA500 OPI2000 PCP25 THC50
• 00870266000461: AMP500 COC150 MET500 MDMA500 OPI2000 THC50
• 00870266000423: AMP1000 COC300 MET1000 OPI2000 THC50
• 00870266000416: AMP1000 COC300 OPI2000 PCP25 THC50