gudid
Primary ID: TytoPro G2
TytoPro (UDI TytoPro G2)
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
Device Regulatory Overview
The TytoPro (Model/Catalog Number: TytoPro G2) 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
- Product Code / EMDN
- FLL
- Device Name
- TytoPro used for comprehensive remote exam and telehealth.This is a convenience kit containing the following DIs: 07290016672787 Tyto Device (with Tyto Thermometer and Tyto Exam Camera), 07290016672817 Tyto Stethoscope and 07290016672824 Tyto Otoscope.TytoPro kits are shipped to the US in a logistic carton labeled with DI 17290016672753 when packed in 6 pack and with 27290016672750 when packed in 48 pack.
- 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.
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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