eudamed_udi
Primary ID: 10889950147624
Hu-Friedy (UDI 10889950147624)
Manufactured by Hu-Friedy Manufacturing Co., LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hu-Friedy - Primary ID 10889950147624
Device Regulatory Overview
The Hu-Friedy (Model/Catalog Number: CAKRO-FLEX) is a medical device manufactured by Hu-Friedy Manufacturing Co., LLC. This product is indexed under FDA Product Code / Category Classification L159012 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CAKRO-FLEX
- Product Code / EMDN
- L159012
- Device Name
- Dental Device
- Database Sync Date
- 2026-08-09 16:58:29
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 Hu-Friedy?
The registered manufacturer of record for Hu-Friedy is Hu-Friedy Manufacturing Co., LLC.
What is the Primary UDI-DI identifier for Hu-Friedy?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10889950147624.
What classification code is assigned to this device?
This device is registered under product classification code L159012.
Similar Classification Devices (L159012)
Other Devices by Hu-Friedy Manufacturing Co., LLC
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