MTD 301001

GUDID 15420045500303

Hologic, Inc.

Mycobacterium tuberculosis nucleic acid IVD, kit, nucleic acid technique (NAT)

• Primary Device ID: 15420045500303
• NIH Device Record Key: a057071d-50a0-4c57-9873-ab46fa60b349
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MTD
• Version Model Number: Amplified Mycobacterium Tuberculosis
• Catalog Number: 301001
• Company DUNS: 050579217
• 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: 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

Customer Support Contacts

• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com
• Phone: +1(800)442-9892
• Email: CustomerSupport@hologic.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	15420045500303 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P940034

FDA Product Code

• MWA: SYSTEM, NUCLEIC ACID AMPLIFICATION, MYCOBACTERIUM TUBERCULOSIS COMPLEX

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: 2014-08-06

Devices Manufactured by Hologic, Inc.

• 15420045517394 - Hologic: 2025-09-05 NG Res Primers Analyte Specific Reagent.
• 15420045517400 - Hologic: 2025-09-05 NG Res Probe (FAM) Analyte Specific Reagent.
• 15420045517417 - Hologic: 2025-09-05 NG Res C272T IVT Control (Positive Control).
• 15420045517424 - Hologic: 2025-09-05 NG IVT Wild Type Control (Negative Control).
• 15420045512412 - DEFINITY CERVICAL DILATOR, 5MM: 2025-07-29
• 15420045512429 - DEFINITY CERVICAL DILATOR, 7MM: 2025-07-29
• 15420045512436 - DEFINITY CERVICAL DILATOR, 9MM: 2025-07-29
• 15420045517097 - DIGITAL DIAGNOSTICS SYSTEM: 2025-07-25 Computer to operate the Genius™ Review Station.