gudid
Primary ID: 0015804
PowerFlexx 1.25 (UDI 0015804)
Manufactured by FERNO-WASHINGTON, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PowerFlexx 1.25 - Primary ID 0015804
Device Regulatory Overview
The PowerFlexx 1.25 (Model/Catalog Number: 0015804) is a medical device manufactured by FERNO-WASHINGTON, INC.. This product is indexed under FDA Product Code / Category Classification FPO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0015804
- Product Code / EMDN
- FPO
- Device Name
- PowerFlexx 1.25, Red
- Database Sync Date
- 2026-08-09 09:09:20
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 PowerFlexx 1.25?
The registered manufacturer of record for PowerFlexx 1.25 is FERNO-WASHINGTON, INC..
What is the Primary UDI-DI identifier for PowerFlexx 1.25?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0015804.
What classification code is assigned to this device?
This device is registered under product classification code FPO.
Similar Classification Devices (FPO)
Other Devices by FERNO-WASHINGTON, INC.
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