TLiIQ System

GUDID 15420045500884

Hologic, Inc.

Fibronectin IVD, kit, enzyme immunohistochemistry Fibronectin IVD, kit, enzyme immunohistochemistry

• Primary Device ID: 15420045500884
• NIH Device Record Key: 9266706a-f812-4ad2-8e82-d159a4b3551c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TLiIQ System
• Version Model Number: TLiIQ System Analyzer
• Company DUNS: 018925968
• Company Name: Hologic, Inc.
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	15420045500884 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P920048

FDA Product Code

• LKV: ENZYME IMMUNOASSAY, FETAL FIBRONECTIN

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2014-09-02

On-Brand Devices [TLiIQ System]

• 15420045500884: TLiIQ System Analyzer
• 15420045500877: TLiIQ System