AICARE

GUDID 06970429840577

Multi Drug Screen Test Dipcard

Co-Innovation Biotech Co., Ltd

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• Primary Device ID: 06970429840577
• NIH Device Record Key: 298a5c4c-9205-48e6-83ad-03baaae917eb
• Commercial Distribution Discontinuation: 2019-03-18
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: AICARE
• Version Model Number: Multi Drug Screen Test
• Company DUNS: 421302978
• Company Name: Co-Innovation Biotech 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: true
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970429840577 [Primary]
GS1	26970429840571 [Package]; Package: [10 Units]; Discontinued: 2019-03-18; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K153050

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: 2019-03-26
• Device Publish Date: 2019-03-18

On-Brand Devices [AICARE]

• 26970429843114: THC Screen Test Dipcard
• 06970429840577: Multi Drug Screen Test Dipcard
• 26970429840120: HCG Pregnancy Test Strip