eudamed_udi
Primary ID: 00645517821399
Unspecified Brand (UDI 00645517821399)
Manufactured by Trulife Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 00645517821399
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: SFC193-25-R-K12) is a medical device manufactured by Trulife Inc.. This product is indexed under FDA Product Code / Category Classification Y062409 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SFC193-25-R-K12
- Product Code / EMDN
- Y062409
- Device Name
- K3 Foot with Pyramid
- Database Sync Date
- 2026-08-09 16:28:46
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Trulife Inc..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00645517821399.
What classification code is assigned to this device?
This device is registered under product classification code Y062409.
Similar Classification Devices (Y062409)
Other Devices by Trulife Inc.
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