eudamed_udi
Primary ID: 05690977245952
Pro-Flex® Modular (UDI 05690977245952)
Manufactured by Össur Iceland ehf.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pro-Flex® Modular - Primary ID 05690977245952
Device Regulatory Overview
The Pro-Flex® Modular (Model/Catalog Number: PMD0825RBR) is a medical device manufactured by Össur Iceland ehf.. This product is indexed under FDA Product Code / Category Classification Y062403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PMD0825RBR
- Product Code / EMDN
- Y062403
- Device Name
- BU00046
- Database Sync Date
- 2026-08-09 16:28:44
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 Pro-Flex® Modular?
The registered manufacturer of record for Pro-Flex® Modular is Össur Iceland ehf..
What is the Primary UDI-DI identifier for Pro-Flex® Modular?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05690977245952.
What classification code is assigned to this device?
This device is registered under product classification code Y062403.
Similar Classification Devices (Y062403)
Other Devices by Össur Iceland ehf.
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