eudamed_udi
Primary ID: 03701037301692
Unspecified Brand (UDI 03701037301692)
Manufactured by FX Shoulder Solutions
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 03701037301692
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 400-1101) is a medical device manufactured by FX Shoulder Solutions. This product is indexed under FDA Product Code / Category Classification P09010303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 400-1101
- Product Code / EMDN
- P09010303
- Device Name
- 3-4 PEGS GLENOID PE CEMENTED SIZE XS
- Database Sync Date
- 2026-08-09 17:46:37
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 FX Shoulder Solutions.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701037301692.
What classification code is assigned to this device?
This device is registered under product classification code P09010303.
Similar Classification Devices (P09010303)
Other Devices by FX Shoulder Solutions
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