Quicksilver Scientific Inc

GUDID 00810147500260

Mercury Tri Test Blood Metal Panel Sample Collection Kit • 4 sample labels • 2 absorbent cloths • 2 biohazard zip-top specimen bags • 2 blood collection tubes • 1 urine collection tube • 1 urine collection cup • 1 hair collection bag • 1 Quicksilver sample box for shipping • Patient requisition form • 1 laboratory shipping pak • 1 Prepaid 2-Day Air Shipping Label

Quicksilver Scientific, Inc.

Drug-testing specimen collection kit IVD

• Primary Device ID: 00810147500260
• NIH Device Record Key: b6cbb41f-6e6b-4f31-b1d5-200ccde2021c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Quicksilver Scientific Inc
• Version Model Number: 1
• Company DUNS: 603214961
• Company Name: Quicksilver Scientific, Inc.
• 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: 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810147500260 [Primary]

FDA Product Code

• NNK: Container, Specimen Mailer And Storage, Non-Sterile

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: 2024-09-02
• Device Publish Date: 2024-08-23