eudamed_udi
Primary ID: 00810028737778
Google Irregular Rhythm Notifications (UDI 00810028737778)
Manufactured by Fitbit LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Google Irregular Rhythm Notifications - Primary ID 00810028737778
Device Regulatory Overview
The Google Irregular Rhythm Notifications (Model/Catalog Number: GA13099) is a medical device manufactured by Fitbit LLC. This product is indexed under FDA Product Code / Category Classification Z12050382 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GA13099
- Product Code / EMDN
- Z12050382
- Device Name
- Fitbit Irregular Rhythm Notifications
- Database Sync Date
- 2026-08-09 17:36:10
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Google Irregular Rhythm Notifications?
The registered manufacturer of record for Google Irregular Rhythm Notifications is Fitbit LLC.
What is the Primary UDI-DI identifier for Google Irregular Rhythm Notifications?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00810028737778.
What classification code is assigned to this device?
This device is registered under product classification code Z12050382.
Similar Classification Devices (Z12050382)
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