gudid
Primary ID: TytoPro G2 US
TytoPro (UDI TytoPro G2 US)
Manufactured by TYTO CARE LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TytoPro - Primary ID TytoPro G2 US
Device Regulatory Overview
The TytoPro (Model/Catalog Number: TytoPro G2 US) is a medical device manufactured by TYTO CARE LTD. This product is indexed under FDA Product Code / Category Classification FLL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TytoPro G2 US
- Product Code / EMDN
- FLL
- Device Name
- Designed for professional use, TytoPro used for comprehensive remote exam and telehealth.The TytoPro includes the Tyto Otoscope, Tyto Stethoscope, Tyto Exam Camera, Tyto Thermometer and disposable ear caps and tongue depressor blades.This is a convenience kit containing the following DIs: 07290016672534 Tyto Device (with Tyto Thermometer and Tyto Exam Camera), 07290016672343 Tyto Stethoscope and 07290016672350 Tyto Otoscope.TytoPro kits are shipped to the US in a 6 pack logistic carton labeled with DI 17290016672548 and 48 pack logistic carton labeled with 27290016672545.
- Database Sync Date
- 2026-08-09 09:18:18
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 TytoPro?
The registered manufacturer of record for TytoPro is TYTO CARE LTD.
What is the Primary UDI-DI identifier for TytoPro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TytoPro G2 US.
What classification code is assigned to this device?
This device is registered under product classification code FLL.
Similar Classification Devices (FLL)
Other Devices by TYTO CARE LTD
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