FDA UDI In Commercial Distribution 🇺🇸 United States

Irregular Rhythm Notification feature 2.0

DI: 00194252456774 · Model: Feature Version 2.x · APPLE INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Irregular Rhythm Notification feature 2.0
Primary DI
00194252456774
Version / Model
Feature Version 2.x
Company Name
APPLE INC.
Labeler DUNS
060704780
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-03-14
Public Version
1
Public Version Date
2022-03-22
Public Version Status
New
Public Device Record Key
8d8d9c39-a9d2-4ad2-b16b-738b1c53d626

Device Description

Irregular Rhythm Notification feature Watch App (Version 2.0)

Device Characteristics

Single Use
No
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
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
QDB Photoplethysmograph Analysis Software For Over-The-Counter Use

GMDN Terms

Code Name
58884 Self-care monitoring/reporting software

Identifiers

Type ID
Primary 00194252456774

Premarket Submissions

Submission Number Supplement Number
K212516 000