Number 1 NIT-1126-P

GUDID 00850040879162

12-Panel Drug Test Cup: AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, PCP, TCA, THC

DEUS VULT, LLC

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• Primary Device ID: 00850040879162
• NIH Device Record Key: be5a8261-416b-4838-814c-ac77681f8fe5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Number 1
• Version Model Number: NIT-1126-P
• Catalog Number: NIT-1126-P
• Company DUNS: 086645029
• Company Name: DEUS VULT, LLC
• 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: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com
• Phone: 866-876-6355
• Email: cs@PreferredMedSupply.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850040879162 [Primary]
GS1	00850040879179 [Package]; Package: Box [25 Units]; In Commercial Distribution
GS1	00850040879186 [Package]; Contains: 00850040879179; Package: Case [4 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131811

FDA Product Code

• LDJ: Enzyme Immunoassay, Cannabinoids

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: 2024-02-09
• Device Publish Date: 2024-02-01

Devices Manufactured by DEUS VULT, LLC

• 00850040879162 - Number 1: 2024-02-0912-Panel Drug Test Cup: AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, PCP, TCA, THC
• 00850040879162 - Number 1: 2024-02-09 12-Panel Drug Test Cup: AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, PCP, TCA, THC
• 00860004081661 - P33: 2022-01-07 10 Panel Drug Test Cup – AMP, BZO, BUP, COC, MET, MTD, MDMA, OPI, OXY, THC
• 00860004081609 - Preferred Med Supply: 2021-08-19 Multi-panel Drug Test Cup