Exploro 7-Panel Urine Drug Test MDP-1074

GUDID 06974246461281

Safecare Biotech (Hangzhou) Co., Ltd.

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• Primary Device ID: 06974246461281
• NIH Device Record Key: e13a4f66-e016-44b7-afd5-02876e7396ee
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Exploro 7-Panel Urine Drug Test
• Version Model Number: 3 tests
• Catalog Number: MDP-1074
• Company DUNS: 544349634
• Company Name: Safecare Biotech (Hangzhou) Co., Ltd.
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	06974246461281 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201120

FDA Product Code

• NFT: Test, Amphetamine, 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: 2024-04-02
• Device Publish Date: 2024-03-25

On-Brand Devices [Exploro 7-Panel Urine Drug Test]

• 06974246461298: 2 tests
• 06974246461281: 3 tests
• 06974246461274: 7 tests
• 06974246461267: 10 tests
• 06974246461250: 15 tests