Identify Fentanyl Rapid Cassette ID-AT1-DIP-FEN-1-AZ1

GUDID 06936983149426

1T,EN,FDA, OTC,1ng

Hangzhou AllTest Biotech Co., Ltd.

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• Primary Device ID: 06936983149426
• NIH Device Record Key: 2b1cf06e-0cd9-44a5-9135-899368b7f280
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Identify Fentanyl Rapid Cassette
• Version Model Number: DFY-A102H A3218
• Catalog Number: ID-AT1-DIP-FEN-1-AZ1
• Company DUNS: 543254717
• Company Name: Hangzhou AllTest Biotech Co., Ltd.
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06936983149426 [Primary]

FDA Product Code

• DJG: Enzyme Immunoassay, Opiates

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: 2024-02-16
• Device Publish Date: 2024-02-08

On-Brand Devices [Identify Fentanyl Rapid Cassette]

• 06936983149433: 25T,EN,FDA clia waived,1ng
• 06936983149426: 1T,EN,FDA, OTC,1ng