23andMe, Inc. Personal Genome Service®(PGS)

Basic Information

• Brand Name: 23andMe, Inc. Personal Genome Service®(PGS)
• Primary DI: 00859462006118
• Version / Model: YouDot
• Catalog Number: n/a
• Company Name: 23ANDME, INC.
• Labeler DUNS: 780119710
• Distribution Status: Not in Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2019-06-27
• Public Version: 4
• Public Version Date: 2021-11-23
• Public Version Status: Update
• Public Device Record Key: c28b71a5-ca74-4bb1-a132-a698b6154b86
• Distribution End Date: 2020-03-10

Device Description

23andMe Personal Genome Service® (PGS) Includes : Carrier Status Report Genetic Health Risk Reports Cancer Predisposition Risk Assessment System (BRCA1/BRCA2 Selected Variants, MUTYH-Associated Polyposis(MAP))

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• 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: No
• Has Manufacturing Date: No
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
PTA	Genetic Variant Detection And Health Risk Assessment System	Immunology	866.5950	2
PKB	Autosomal Recessive Carrier Screening Gene Mutation Detection System	Immunology	866.5940	2
QAZ	Cancer Predisposition Risk Assessment System For Brca1/Brca2 Select Variants	Medical Genetics	866.6090	2

GMDN Terms

Code	Name	Definition	Implantable	Status
61777	Human genomic analysis interpretive software	An interpretive software program intended to be used for the analysis and visualization of human genome data from in vitro diagnostic (IVD) results obtained through molecular genetic testing (e.g., whole genome, targeted genome, or exome analyses). It provides predictive and/or diagnostic information (e.g., gene-drug associations, congenital and/or acquired aneuploidy status, genotype-phenotype relationships) used by a professional in the assessment of patient adverse health condition risk, disease prevention, and/or health management, or for lifestyle guidance as pertains to a patient genomic profile. This software is not an IVD device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00859462006118	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]