FastPack® IP Total PSA Kit (90) 25000057

GUDID 30816467020014

90 Test Ported TPSA Immunoassay Kit

QUALIGEN INC.

Total prostate specific antigen (tPSA) IVD, kit, chemiluminescent immunoassay

• Primary Device ID: 30816467020014
• NIH Device Record Key: fa4af732-a206-4823-9c82-d1e6ea4f5a51
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FastPack® IP Total PSA Kit (90)
• Version Model Number: TPSA Immunoassay
• Catalog Number: 25000057
• Company DUNS: 959103565
• Company Name: QUALIGEN INC.
• Device Count: 90
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: false

Customer Support Contacts

• Phone: 1-877-770-6127
• Email: systemsupport@qualigeninc.com
• Phone: 1-877-770-6127
• Email: systemsupport@qualigeninc.com

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius
• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816467020013 [Unit of Use]
GS1	30816467020014 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K003094

FDA Product Code

• LTJ: Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-06
• Device Publish Date: 2017-09-14

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