FDA UDI In Commercial Distribution 🇺🇸 United States

GENIUS AI DETECTION

DI: 15420045512474 · Model: GENIUS AI DETECTION SOFTWARE · Hologic, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
GENIUS AI DETECTION
Primary DI
15420045512474
Version / Model
GENIUS AI DETECTION SOFTWARE
Catalog Number
ASY-15431
Company Name
Hologic, Inc.
Labeler DUNS
139534114
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-12-01
Public Version
3
Public Version Date
2025-02-24
Public Version Status
Update
Public Device Record Key
9e9aa535-f885-4da8-b35b-5d205d952ffb

Device Description

Genius AI® is a computer-aided detection and diagnosis (CADe/CADx) software device intended to be used with compatible digital breast tomosynthsis (DBT) systems to identify and mark regions of interest including soft tissue densities (masses, architectural distortions, and assymetries) and calcifications in DBT exams from compatible DBT systems and provide confidence scores that offer assessment for Certainty of Findings and a Case Score.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OTE Digital breast tomosynthesis

GMDN Terms

Code Name
37672 Stationary mammographic x-ray system, digital

Identifiers

Type ID
Primary 15420045512474

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P080003 008

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-10 – 40 Degrees Celsius