gudid
Primary ID: PT3
iHealth (UDI PT3)
Manufactured by iHealth Labs Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for iHealth - Primary ID PT3
Device Regulatory Overview
The iHealth (Model/Catalog Number: PT3) is a medical device manufactured by iHealth Labs Inc.. This product is indexed under FDA Product Code / Category Classification SDV within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PT3
- Product Code / EMDN
- SDV
- Device Name
- Database Sync Date
- 2026-08-09 09:37:40
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 iHealth?
The registered manufacturer of record for iHealth is iHealth Labs Inc..
What is the Primary UDI-DI identifier for iHealth?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PT3.
What classification code is assigned to this device?
This device is registered under product classification code SDV.
Similar Classification Devices (SDV)
Other Devices by iHealth Labs Inc.
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