Trident Specimen Radiography System RM-ASY-04823

GUDID 15420045505919

Hologic, Inc.

Stationary mammographic x-ray system, digital

• Primary Device ID: 15420045505919
• NIH Device Record Key: c7086347-b98b-4b98-b463-ab24f95ce5b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Trident Specimen Radiography System
• Version Model Number: RM-ASY-04823
• Catalog Number: RM-ASY-04823
• Company DUNS: 139534114
• Company Name: Hologic, Inc.
• Device Count: 1
• DM Exempt: false
• 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: true
• 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	15420045505919 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111508

FDA Product Code

• MWP: Cabinet,x-ray system

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: 2017-04-08

On-Brand Devices [Trident Specimen Radiography System]

• 15420045505919: RM-ASY-04823
• 15420045505902: ASY-04212
• 15420045505841: ASY-04823